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FDA Inspection
•Keller Laboratories•June 22, 2012

FDA Inspection 787218 - Keller Laboratories - June 22, 2012

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Record Details

This FDA Inspection record concerns Keller Laboratories, with an inspection on June 22, 2012, issued by the Center for Devices and Radiological Health, covering devices.

Company
Keller Laboratories
Inspection Date
June 22, 2012
Product Type
Devices
Office
Center for Devices and Radiological Health
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ID · 56ba50c2-c068-42ea-9cfd-b2398e6905fe

Violation Codes2
21 CFR 820.100(a)21 CFR 820.40(a)

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