FDA Inspection 1293744 — Mercury Enterprises, Inc.

Mercury Enterprises, Inc. — FEI 1024404

The FDA completed an inspection of Mercury Enterprises, Inc. on December 11, 2025 in Clearwater, FL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
December 11, 2025
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
Clearwater, FL (United States)

Citations

IDCFRDescription
312121 CFR 820.80(b)Lack of or inadequate receiving acceptance procedures
313021 CFR 820.100(a)Lack of or inadequate procedures