FDA Inspection 800605 — McKesson Corporation
The FDA completed an inspection of McKesson Corporation on October 1, 2012 in Everett, WA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 3 citations were issued during this inspection. Product area: Drugs.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- October 1, 2012
- Fiscal Year
- 2013
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Everett, WA (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 1112 | 21 CFR 211.25(a) | Training--operations, GMPs, written procedures |
| 1261 | 21 CFR 211.68(a) | Written calibration / inspection records not kept |
| 4342 | 21 CFR 211.142(b) | Storage under appropriate conditions |