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FDA Inspection 903287 — Prestige Ameritech

Prestige Ameritech — FEI 3005022483

The FDA completed an inspection of Prestige Ameritech on November 13, 2014 in North Richland Hills, TX. 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
November 13, 2014
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
North Richland Hills, TX (United States)

Facility

Other inspections at this facility

  • 1084042 (VAI Wed Mar 27 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1063422 (VAI Mon Aug 20 2018 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources