FDA Inspection 1115810 — Mid South Precision, Inc.
The FDA completed an inspection of Mid South Precision, Inc. on Jan 22, 2020 in Murfreesboro, TN. 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
- Jan 22, 2020
- Fiscal Year
- 2020
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Murfreesboro, TN (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 3120 | 21 CFR 820.80(a) | Lack of or inadequate procedures - Acceptance activities |
| 3130 | 21 CFR 820.100(a) | Lack of or inadequate procedures |
| 3282 | 21 CFR 820.90(a) | Nonconforming product, Lack of or inadequate procedures |
| 3698 | 21 CFR 820.150(b) | Procedures - receipt and dispatch |
| 479 | 21 CFR 820.50 | Purchasing controls, Lack of or inadequate procedures |