FDA Inspection
Mid South Precision, Inc.Mid South Precision, Inc. – FDA Inspection, Apr 26, 2024
Record Details
This FDA Inspection record concerns Mid South Precision, Inc., with an inspection on April 26, 2024, issued by the Center for Devices and Radiological Health, covering devices.
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ID · 6acd163a-50de-432e-a46a-4de20eed8c80
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1237096
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
5- 21 CFR 820.72(a)Calibration, Inspection, etc. Procedures Lack of or Inadequ
- 21 CFR 820.184Lack of or inadequate DHR procedures
- 21 CFR 820.75(a)Lack of or inadequate process validation
- 21 CFR 820.90(b)(2)Product rework procedures, Lack of or inadequate procedures
- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
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Other FDA inspections of Mid South Precision, Inc.
4| Date | Classification | Office | Project area |
|---|---|---|---|
| May 12, 2025 | VAI | New Orleans District Office | Compliance: Medical Devices |
| October 25, 2021 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| January 22, 2020 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| October 16, 2017 | Not classified | New Orleans District Office | Compliance: Devices |
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