FDA Inspection 675749 - Perma Pure LLC - August 23, 2010

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Record Details

This FDA Inspection record concerns Perma Pure LLC, with an inspection on August 23, 2010, issued by the Center for Devices and Radiological Health, covering devices.

Company: Perma Pure LLC
Inspection Date: August 23, 2010
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · b183f8b8-631f-4036-b75a-77a89ab4c3c1

Violation Codes10

21 CFR 803.1721 CFR 820.100(a)21 CFR 820.18421 CFR 820.198(a)21 CFR 820.20(c)21 CFR 820.250(b)21 CFR 820.4021 CFR 820.70(g)(1)21 CFR 820.70(i)21 CFR 820.72(a)

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