FDA Inspection 864181 - PROMEPLA - December 12, 2013

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Record Details

This FDA Inspection record concerns PROMEPLA, with an inspection on December 12, 2013, issued by the Center for Devices and Radiological Health, covering devices.

Company: PROMEPLA
Inspection Date: December 12, 2013
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 6f888c99-ae61-4eb0-a5b1-9d19c158b4d0

Violation Codes5

21 CFR 820.100(a)21 CFR 820.100(b)21 CFR 820.198(a)21 CFR 820.25(b)21 CFR 820.70(c)

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