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FDA Inspection
•AmerisourceBergen Drug Corporation•October 7, 2008

AmerisourceBergen Drug Corporation – FDA Inspection, Oct 7, 2008

Record Details

This FDA Inspection record concerns AmerisourceBergen Drug Corporation, with an inspection on October 7, 2008, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
AmerisourceBergen Drug Corporation
Inspection Date
October 7, 2008
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · 87de9b52-c605-4470-83ec-a8882d0d60f3

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
542388
FDA center
Human Drugs
Project area
Drug Quality Assurance

FDA Citations

3
  1. 21 CFR 211.142(b)Storage under appropriate conditions
  2. 21 CFR 211.204Returned drug products with doubt cast as to safety et. al.
  3. 21 CFR 211.68(a)Calibration/Inspection/Checking not done

Full citation text and observation details available on the Dashboard.

Other FDA inspections of AmerisourceBergen Drug Corporation

2
DateClassificationOfficeProject area
December 4, 2025Not classifiedSeattle District Office
December 29, 2017Not classifiedSeattle District Office
Other documents for AmerisourceBergen Drug Corporation
  • FDA Inspection 1284153 - 2025-12-04
  • FDA Inspection 1037790 - 2017-12-29

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