FDA Inspection 1166532 — Bio-Med Devices, Inc.
The FDA completed an inspection of Bio-Med Devices, Inc. on Mar 31, 2022 in Guilford, CT. 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). 2 citations were issued during this inspection. Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Mar 31, 2022
- Fiscal Year
- 2022
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Guilford, CT (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 3128 | 21 CFR 820.90(a) | Nonconforming product control |
| 3139 | 21 CFR 820.140 | Lack of or inadequate procedures for handling |