FDA Inspection 912665 — Weiman Products, LLC
The FDA completed an inspection of Weiman Products, LLC on January 29, 2015 in Gurnee, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 3 citations were issued during this inspection. Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- January 29, 2015
- Fiscal Year
- 2015
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Gurnee, IL (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 2386 | 21 CFR 110.80(a)(1) | Storage |
| 3668 | 21 CFR 820.20(c) | Management review dates |
| 4057 | 21 CFR 820.20(a) | Management ensuring quality policy is understood |