FDA Inspection 775770 — Barton-Carey Medical Products Inc

Barton-Carey Medical Products Inc — FEI 3003070670

The FDA completed an inspection of Barton-Carey Medical Products Inc on Apr 3, 2012 in Jellico, TN. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Apr 3, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Jellico, TN (United States)

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