FDA Inspection 1273998 — Barton-Carey Medical Products Inc

Barton-Carey Medical Products Inc — FEI 3003070670

The FDA completed an inspection of Barton-Carey Medical Products Inc on May 20, 2025 in Jellico, TN. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
May 20, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Jellico, TN (United States)