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FDA Inspection 1018344 — Tingle X-Ray Products Inc

Tingle X-Ray Products Inc — FEI 3002539637

The FDA completed an inspection of Tingle X-Ray Products Inc on June 23, 2017 in Cottondale, AL. 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
June 23, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Cottondale, AL (United States)

Facility

Other inspections at this facility

  • 887526 (NAI Thu Jul 17 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 823246 (VAI Fri Mar 22 2013 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources