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Keller Laboratories 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 3006650414.

Keller Laboratories

Fenton, Missouri, United States
Issue DateJune 22, 2012
FEI Number3006650414
CountryUnited States
Status
No Warning Letter
Product Type
Devices
Keller Laboratories FDA Form 483, Fenton, Missouri, June 22, 2012