FDA Inspection 720685 — 3M Company
The FDA completed an inspection of 3M Company on Apr 13, 2011 in Cordova, IL. 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). 4 citations were issued during this inspection. Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Apr 13, 2011
- Fiscal Year
- 2011
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Cordova, IL (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 1105 | 21 CFR 211.22(d) | Procedures not in writing, fully followed |
| 1384 | 21 CFR 211.101(c) | Weighing/measuring/subdividing supervision |
| 4323 | 21 CFR 211.115(a) | Reprocessing procedures lack steps to be taken |
| 4576 | 21 CFR 211.192 | No written record of investigation |