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Peter Kosek 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 3004777404.

Peter Kosek

Springfield, Oregon, United States
Issue DateApril 21, 2017
FEI Number3004777404
CountryUnited States
Status
No Warning Letter
Product Type
Devices
Peter Kosek FDA Form 483, Springfield, Oregon, April 21, 2017