FDA Inspection
Mid South Precision, Inc.Mid South Precision, Inc. – FDA Inspection, Oct 25, 2021
Record Details
This FDA Inspection record concerns Mid South Precision, Inc., with an inspection on October 25, 2021, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Mid South Precision, Inc.
- Inspection Date
- October 25, 2021
- Product Type
- Devices
View Company Profile
ID · c4face3a-73e2-44ce-8fbe-527abfc63db5
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1155220
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
3- 21 CFR 820.80(e)Documentation
- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.50(a)Evaluation of suppliers, contractors, etc., requirements
Full citation text and observation details available on the Dashboard.
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 |
| April 26, 2024 | 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 |
Other documents for Mid South Precision, Inc.
Document or profile
One record shows the event. A profile shows the pattern.
Buy this document for the source file and details behind this single event.
Choose full profile access to connect related records, sites, people, citations, and enforcement history in one view.