FDA Inspection
Mid South Precision, Inc.Mid South Precision, Inc. – FDA Inspection, Oct 16, 2017
Record Details
This FDA Inspection record concerns Mid South Precision, Inc., with an inspection on October 16, 2017, issued by the New Orleans District Office, covering medical devices & rad health.
- Company
- Mid South Precision, Inc.
- Inspection Date
- October 16, 2017
- Product Type
- Medical Devices & Rad Health
- Person
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ID · 8ccc531a-ad5f-4625-9b4e-ad09f14f8792
Inspection Facts
- Inspection number
- 1028711
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
7- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.181DMR - not or inadequately maintained
- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
- 21 CFR 820.50Purchasing controls, Lack of or inadequate procedures
- 21 CFR 820.75(a)Lack of or inadequate process validation
- 21 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures
- 21 CFR 820.90(b)(2)Product rework documentation, DHR {see also 820.184}
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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 |
| April 26, 2024 | VAI | Center for Devices and Radiological Health | Compliance: 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 |
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