FDA Inspection
McKesson CorporationMcKesson Corporation – FDA Inspection, Dec 11, 2009
Record Details
This FDA Inspection record concerns McKesson Corporation, with an inspection on December 11, 2009, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- McKesson Corporation
- Inspection Date
- December 11, 2009
- Product Type
- Drugs
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ID · 5b73b2e1-cfe3-4f43-847a-2f5e52405edc
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 633482
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
3- 21 CFR 211.150(b)Recall facilitation
- 21 CFR 211.198(b)Maintenance of Complaint File
- 21 CFR 211.25(a)GMP Training Frequency
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Other FDA inspections of McKesson Corporation
2| Date | Classification | Office | Project area |
|---|---|---|---|
| April 25, 2023 | Not classified | Kansas City District Office | |
| August 2, 2018 | NAI | Center for Food Safety and Applied Nutrition | Foodborne Biological Hazards |
Other documents for McKesson Corporation
- FDA Inspection 1204494 - 2023-04-25
- FDA Inspection 1070470 - 2018-08-02
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