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Prestige Ameritech Form 483 Details

Form 483
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Source: FDA inspection recordConfirmed against FDA's published inspection data for this establishment and inspection date. FDA has published the inspection and what it cited, but not the form itself, which usually takes six to twelve months.

To check this against FDA, open FDA's record for this establishment on FDA's Data Dashboard, which lists this inspection under FEI 3005022483.

Prestige Ameritech

North Richland Hills, Texas, United States
Issue DateAugust 20, 2018
FEI Number3005022483
CountryUnited States
Status
No Warning Letter
Product Type
Devices
Prestige Ameritech FDA Form 483, North Richland Hills, Texas, August 20, 2018