FDA Inspection 576581 — Smith & Nephew, Inc.
The FDA completed an inspection of Smith & Nephew, Inc. on Apr 23, 2009 in Memphis, TN. 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: Devices.
Inspection details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Apr 23, 2009
- Fiscal Year
- 2009
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Memphis, TN (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 3201 | 21 CFR 820.40(a) | Not approved or obsolete document retrieval |
| 3690 | 21 CFR 820.100(a)(3) | Identification of actions needed |
| 4189 | 21 CFR 820.198(a) | General |