FDA Inspection
McKesson CorporationMcKesson Corporation – FDA Inspection, Oct 1, 2012
Record Details
This FDA Inspection record concerns McKesson Corporation, with an inspection on October 1, 2012, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- McKesson Corporation
- Inspection Date
- October 1, 2012
- Product Type
- Drugs
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ID · e32dc46f-c72b-4743-93c9-f944652812f5
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 800605
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
3- 21 CFR 211.142(b)Storage under appropriate conditions
- 21 CFR 211.25(a)Training--operations, GMPs, written procedures
- 21 CFR 211.68(a)Written calibration / inspection records not kept
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Other FDA inspections of McKesson Corporation
1| Date | Classification | Office | Project area |
|---|---|---|---|
| September 11, 2017 | NAI | Center for Food Safety and Applied Nutrition | Foodborne Biological Hazards |
Other documents for McKesson Corporation
- FDA Inspection 1029192 - 2017-09-11
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