FDA Inspection 1086270 — Deringer-Ney, Inc.
The FDA completed an inspection of Deringer-Ney, Inc. on April 12, 2019 in Bloomfield, CT. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- April 12, 2019
- Fiscal Year
- 2019
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Bloomfield, CT (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 3239 | 21 CFR 820.72(b) | Remedial action - documentation |
| 3837 | 21 CFR 820.25(b) | Training records |