FDA Inspection 633482 — McKesson Corporation
The FDA completed an inspection of McKesson Corporation on Dec 11, 2009 in O Fallon, MO. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 3 citations were issued during this inspection. Product area: Drugs.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Dec 11, 2009
- Fiscal Year
- 2010
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- O Fallon, MO (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 1133 | 21 CFR 211.25(a) | GMP Training Frequency |
| 2569 | 21 CFR 211.198(b) | Maintenance of Complaint File |
| 4338 | 21 CFR 211.150(b) | Recall facilitation |