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Primus Sterilizer Co Inc 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 1000119270.

Primus Sterilizer Co Inc

Great Bend, Kansas, United States
Issue DateFebruary 21, 2017
FEI Number1000119270
CountryUnited States
Status
No Warning Letter
Product Type
Devices
Primus Sterilizer Co Inc FDA Form 483, Great Bend, Kansas, February 21, 2017