FDA Inspection 1269865 — Mid South Precision, Inc.

Mid South Precision, Inc. — FEI 3011189525

The FDA completed an inspection of Mid South Precision, Inc. on May 12, 2025 in Murfreesboro, TN. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 3 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
May 12, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Murfreesboro, TN (United States)

Citations

IDCFRDescription
313021 CFR 820.100(a)Lack of or inadequate procedures
54121 CFR 820.70(c)Environmental control Lack of or inadequate procedures
54621 CFR 820.75(a)Lack of or inadequate process validation

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.