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Mid South Precision, Inc.

FDA Regulatory Profile

Mid South Precision, Inc. has 0 FDA recalls, 4 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
May 12, 2025 · VAI

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections4Nov 12, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
May 12, 2025Murfreesboro, TNDevicesVoluntary Action Indicated (VAI)3011189525
Apr 26, 2024Murfreesboro, TNDevicesVoluntary Action Indicated (VAI)3011189525
Oct 25, 2021Murfreesboro, TNDevicesVoluntary Action Indicated (VAI)3011189525
Jan 22, 2020Murfreesboro, TNDevicesVoluntary Action Indicated (VAI)3011189525

NAI means no objectionable conditions or practices were found during the inspection. VAI means objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action. OAI means regulatory and/or administrative actions are recommended.

Look up the inspector observations behind these results with the FDA 483 search, or check for formal enforcement with the FDA warning letter search.

FDA-Inspected Facilities

FacilityLocationInspectionsLatest
FEI 3011189525Murfreesboro, TN4May 12, 2025

FDA data resources

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