Practice Chapter 5 Thru 8 Review Quiz

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1. Which agency may intervene in a matter of worker protection even if there are no specific regulations covering the situation?

Explanation

The correct answer is OSHA because it is responsible for ensuring safe and healthy working conditions for workers, even in situations where specific regulations may not exist.

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Practice Chapter 5 Thru 8 Review Quiz - Quiz

Enhance your understanding of chapters 5 through 8 with our focused review flashcards. This tool aids in revising key concepts and learning effectively, making it ideal for students... see moreseeking to consolidate their knowledge in a structured manner. see less

2. Which agency administers regulations under the Clean Air Act?

Explanation

The Environmental Protection Agency (EPA) is responsible for administering regulations under the Clean Air Act to protect human health and the environment from the harmful effects of air pollution.

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3. Which agency imposes very strict labeling requirements on manufacturers of chemicals used by Central Service departments?

Explanation

The Environmental Protection Agency (EPA) is responsible for imposing very strict labeling requirements on manufacturers of chemicals used by Central Service departments. OSHA focuses on workplace safety standards, FDA regulates food and drug products, and AAMI sets standards for medical equipment.

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4. Healthcare regulations and standards provide consistency of departmental activites by outlining..

Explanation

Healthcare regulations and standards focus on setting minimum performance standards to ensure quality and consistency in departmental activities. Equal pay practices and productivity timelines may be important aspects in healthcare management, but they are not the primary focus of regulations and standards.

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5. Are established national emissions standards for EO used by hospitals regulated?

Explanation

The correct answer is D because there are currently no established national emission standards for EO used by hospitals. This means that the regulation of emissions standards for EO varies across different states and regions.

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6. Chemical indicators are FDA regulated devices.

Explanation

Chemical indicators are classified as Class II medical devices by the FDA, indicating a moderate to high risk level.

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7. Heart valves and pacemakers are examples of FDA regulated medical devices. What class of medical device are they?

Explanation

Class III devices are those for which insufficient information exists to assure safety and effectiveness solely through the general or special controls sufficient for Class I or Class II devices. These devices usually require premarket approval (PMA) from the FDA before marketing.

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8. Under current regulations who is required to report suspected medical device-related deaths to the FDA?

Explanation

According to current regulations, both device manufacturers and hospitals are required to report suspected medical device-related deaths to the FDA. Therefore, the correct answer is 'C. All of the above'.

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9. Standards and regulations help set levels of what in our departments?
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10. Medical Device reporting is regulated by the:

Explanation

Medical device reporting is mandated by the FDA as part of its regulation to ensure the safety and effectiveness of medical devices in the market. The FDA requires manufacturers, importers, and device user facilities to report certain device-related adverse events and product problems.

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11. When state or local regulations differ from Federal regulations, the most lenient regulations apply.

Explanation

In cases where state or local regulations differ from Federal regulations, the most stringent regulations always apply to ensure the highest level of compliance and safety.

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12. According to OSHA regulations, wearing PPE in the Central Service Decontamination area is optional.

Explanation

According to OSHA regulations, wearing PPE in the Central Service Decontamination area is mandatory to ensure the safety of workers and prevent exposure to hazardous materials.

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13. Are Third Party Reprocessors regulated by the FDA?

Explanation

Third Party Reprocessors are indeed regulated by the FDA to ensure compliance with quality and safety standards.

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14. Recommendations regarding sterilization practices are provided by AAMI (Association for the Advancement of Medical Instrumentation).

Explanation

AAMI indeed provides recommendations on sterilization practices in the medical field, making the statement true. The organization plays a crucial role in establishing standards for medical equipment and practices.

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15. ANSI (American National Standards Institute) is a voluntary association dedicated to infection control and prevention.

Explanation

ANSI (American National Standards Institute) is not dedicated to infection control and prevention, but rather to promoting and facilitating voluntary consensus standards and ensuring their integrity.

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16. The organization that conducts on-site surveys to evaluate healthcare organizations is the ISO (International Standards Organization).

Explanation

The correct organization that conducts on-site surveys to evaluate healthcare organizations is not the ISO (International Standards Organization), but rather agencies like the WHO (World Health Organization), FDA (Food and Drug Administration), and CDC (Centers for Disease Control and Prevention).

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17. Failure to receive accreditation from the joint commission can result in the loss of medicare and medicaid payments.

Explanation

Accreditation from the Joint Commission is crucial for healthcare organizations to maintain eligibility for receiving Medicare and Medicaid payments. Not having accreditation can indeed lead to the loss of these payments.

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18. The SGNA (Society of Gastroenterology Nurses and Associates) is a good source for information about the proper processing of flexible endoscopes.

Explanation

The SGNA is indeed a reputable source for information on the proper processing of flexible endoscopes. The organization provides guidelines and resources to ensure the safety and effectiveness of endoscope procedures.

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19. Class III medical devices are identified as High Risk.

Explanation

Class III medical devices are indeed identified as High Risk according to medical device classification rules. These types of devices are those that support or sustain human life, are of substantial importance in preventing impairment of human health, or present a potential unreasonable risk of illness or injury.

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20. Re-use of single use medical devices is less regulated now than it was in the 1990's.

Explanation

The correct answer is False because re-use of single use medical devices is actually more regulated now than it was in the 1990's to ensure patient safety and prevent the spread of infections.

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21. Each year, approximately how many patients develop a healthcare-associated infection?

Explanation

Healthcare-associated infections are a major concern in the medical field, affecting millions of patients each year. The correct estimate is around 2 million cases annually.

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22. Watches and other jewelry should not be worn in the Central Service department work areas because:

Explanation

Watches and jewelry should not be worn in the Central Service department work areas primarily because they can harbor bacteria which poses a risk to patient safety and infection control.

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23. During handwashing, hands should be lathered and scrubbed for at least:

Explanation

Proper handwashing technique involves lathering and scrubbing hands for at least 15 seconds to effectively remove dirt, germs, and other contaminants. Washing for shorter durations may not be sufficient to properly clean hands, while washing for longer durations may lead to dryness or irritation.

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24. To protect themselves from splashes and spills, Central Service Technicians assigned to the decontamination area should wear:

Explanation

Central Service Technicians need to wear fluid-resistant gowns in the decontamination area to protect themselves from splashes and spills as they provide a higher level of protection against contamination compared to other options.

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25. The main theory of Standards Precautions is that;

Explanation

The main theory of Standards Precautions is that all patients, regardless of whether they have been diagnosed with an infectious disease or not, may pose a risk of infection.

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26. Which of the following is NOT a requirement of the OSHA (Occupational Safety and Health Administration) Bloodborne Pathogen Standard?

Explanation

The OSHA Bloodborne Pathogen Standard does not specifically require biohazard areas to be kept locked. However, it does mandate providing hepatitis B vaccine, observing standard precautions, and using engineering controls to prevent biohazard exposures to ensure workplace safety.

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27. Following Standard Precautions protocols is required by:

Explanation

Standard Precautions in healthcare are recommended infection control practices to prevent transmission of diseases. While organizations like the FDA, NFPA, and EPA may have their own guidelines, OSHA specifically focuses on workplace safety and health regulations.

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28. Who do departmental dress codes apply to in the Central Service department?

Explanation

Departmental dress codes apply to everyone entering the Central Service department to ensure safety and compliance with regulations.

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29. Inanimate objects that can transmit bacteria are called:

Explanation

Fomites are inanimate objects that can harbor and transmit bacteria, contributing to the spread of infections.

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30. How often should floors in the Central Service department be cleaned?

Explanation

It is crucial to wet-mop the floors daily in the Central Service department to maintain cleanliness and prevent the accumulation of dirt and germs.

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Which agency may intervene in a matter of worker protection even if...
Which agency administers regulations under the Clean Air Act?
Which agency imposes very strict labeling requirements on...
Healthcare regulations and standards provide consistency of...
Are established national emissions standards for EO used by hospitals...
Chemical indicators are FDA regulated devices.
Heart valves and pacemakers are examples of FDA regulated medical...
Under current regulations who is required to report suspected medical...
Standards and regulations help set levels of what in our departments?
Medical Device reporting is regulated by the:
When state or local regulations differ from Federal regulations, the...
According to OSHA regulations, wearing PPE in the Central Service...
Are Third Party Reprocessors regulated by the FDA?
Recommendations regarding sterilization practices are provided by AAMI...
ANSI (American National Standards Institute) is a voluntary...
The organization that conducts on-site surveys to evaluate healthcare...
Failure to receive accreditation from the joint commission can result...
The SGNA (Society of Gastroenterology Nurses and Associates) is a good...
Class III medical devices are identified as High Risk.
Re-use of single use medical devices is less regulated now than it was...
Each year, approximately how many patients develop a...
Watches and other jewelry should not be worn in the Central Service...
During handwashing, hands should be lathered and scrubbed for at...
To protect themselves from splashes and spills, Central Service...
The main theory of Standards Precautions is that;
Which of the following is NOT a requirement of the OSHA (Occupational...
Following Standard Precautions protocols is required by:
Who do departmental dress codes apply to in the Central Service...
Inanimate objects that can transmit bacteria are called:
How often should floors in the Central Service department be cleaned?
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