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FDA Inspection
•Mid South Precision, Inc.•May 12, 2025

Mid South Precision, Inc. – FDA Inspection, May 12, 2025

Record Details

This FDA Inspection record concerns Mid South Precision, Inc., with an inspection on May 12, 2025, issued by the New Orleans District Office, covering medical devices & rad health.

Company
Mid South Precision, Inc.
Inspection Date
May 12, 2025
Product Type
Medical Devices & Rad Health
Office
New Orleans District Office
Person
  • Jamie P. Webb (Issuing Officer)
View Company Profile

ID · bc755e7b-76e8-4914-abb9-f2675db828fe

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
1269865
FDA center
Medical Devices & Rad Health
Project area
Compliance: Medical Devices
Outcome
Form 483 issued, view the record

FDA Citations

3
  1. 21 CFR 820.75(a)Lack of or inadequate process validation
  2. 21 CFR 820.100(a)Lack of or inadequate procedures
  3. 21 CFR 820.70(c)Environmental control Lack of or inadequate procedures

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Mid South Precision, Inc.

4
DateClassificationOfficeProject area
April 26, 2024VAICenter for Devices and Radiological HealthCompliance: Devices
October 25, 2021VAICenter for Devices and Radiological HealthCompliance: Devices
January 22, 2020VAICenter for Devices and Radiological HealthCompliance: Devices
October 16, 2017Not classifiedNew Orleans District OfficeCompliance: Devices
Other documents for Mid South Precision, Inc.
  • FDA Inspection 1237096 - 2024-04-26
  • FDA Inspection 1155220 - 2021-10-25
  • FDA Inspection 1115810 - 2020-01-22
  • FDA Inspection 1028711 - 2017-10-16

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