FDA Inspection 808669 - taberna pro medicum - November 01, 2012

Record Details

This FDA Inspection record concerns taberna pro medicum, with an inspection on November 1, 2012, issued by the Center for Devices and Radiological Health, covering devices.

Company: taberna pro medicum
Inspection Date: November 1, 2012
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 590eb90a-1b85-4821-a5ae-81096fd48e54

Violation Codes5

21 CFR 820.18421 CFR 820.198(a)21 CFR 820.2221 CFR 820.30(f)21 CFR 820.90(a)

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