FDA Inspection 781212 — Multi-Med, Inc.
The FDA completed an inspection of Multi-Med, Inc. on May 11, 2012 in Keene, NH. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- May 11, 2012
- Fiscal Year
- 2012
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Keene, NH (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 3270 | 21 CFR 820.80(c) | Documentation |
| 447 | 21 CFR 820.40 | Lack of procedures, or not maintained |