FDA Inspection 787543 - The Prometheus Group - June 21, 2012

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Record Details

This FDA Inspection record concerns The Prometheus Group, with an inspection on June 21, 2012, issued by the Center for Devices and Radiological Health, covering devices.

Company: The Prometheus Group
Inspection Date: June 21, 2012
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · b3e4d91b-5bde-413b-a3dd-63ffd65123f1

Violation Codes2

21 CFR 820.30(g)21 CFR 820.30(j)

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