FDA Inspection 1155220 — Mid South Precision, Inc.

Mid South Precision, Inc. — FEI 3011189525

The FDA completed an inspection of Mid South Precision, Inc. on October 25, 2021 in Murfreesboro, TN. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 3 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
October 25, 2021
Fiscal Year
2022
Product Type
Devices
Project Area
Compliance: Devices
Location
Murfreesboro, TN (United States)

Citations

IDCFRDescription
312721 CFR 820.80(e)Documentation
313021 CFR 820.100(a)Lack of or inadequate procedures
48621 CFR 820.50(a)Evaluation of suppliers, contractors, etc., requirements