FDA Inspection 913129 — Gardner Denver Thomas Inc
The FDA completed an inspection of Gardner Denver Thomas Inc on Feb 6, 2015 in Monroe, LA. 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
- Feb 6, 2015
- Fiscal Year
- 2015
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Monroe, LA (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 3236 | 21 CFR 820.72(b) | Calibration procedures - content |
| 4212 | 21 CFR 806.20(b)(4) | Justification for not reporting |