FDA Inspection 1250031 — Sarasota Medical Products, Inc.

Sarasota Medical Products, Inc. — FEI 3009167225

The FDA completed an inspection of Sarasota Medical Products, Inc. on September 12, 2024 in Sarasota, FL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
September 12, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Sarasota, FL (United States)