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PageSpeed score of Does a laboratory’s responsibility for corrective action listed on a FDA-483 begin at the conclusion of an inspection or upon receipt of correspondence from the originating bureau in which corrective action is requested? page
Does a laboratory’s responsibility for corrective action listed on a FDA-483 begin at the conclusion of an inspection or upon receipt of correspondence from the originating bureau in which corrective action is requested?
The FDA-483 lists observations of violative conditions that have the capability to adversely
affect nonclinical laboratory studies. Corrective actions should be instituted as soon as
possible.