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The validation process is performed by the manufacturing company.

Inadequate exposure time at the correct temperature and pressure will still render an item sterile.

The sterile storage environmental controls should allow for_________________________.

All sterilization methods cycles, especially those that include implants, should have ____________ to ensure the sterilization process is effective.

An aeration time for Eto sterilization would be___________.

A _______________ should be ran in every sterilizer load and then placed into an incubator, to ensure all microorganisms are killed. 

The door is the weakest part of the steam sterilizer.

Sterilized packages may be jeopardized due to the storage practices in the department.

Items located near the drain of the steam autoclave are usually the __________________ to sterilize.

The U.S. Food and Drug Administration Class Il chemical indicator that is run daily in dynamic air removal sterilizers is called a