FDA Inspection 998349 — Gauthier Biomedical, Inc.
The FDA completed an inspection of Gauthier Biomedical, Inc. on Dec 15, 2016 in Grafton, WI. 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). 5 citations were issued during this inspection. Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Dec 15, 2016
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Grafton, WI (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 14713 | 21 CFR 820.198(a) | Lack of or inadequate complaint procedures |
| 3130 | 21 CFR 820.100(a) | Lack of or inadequate procedures |
| 479 | 21 CFR 820.50 | Purchasing controls, Lack of or inadequate procedures |
| 642 | 21 CFR 803.18(b)(1)(i) | Adverse events--all info not in file |
| 650 | 21 CFR 803.18(e) | Results of evaluation not in mfr's MDR file |