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

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 · de0be5b0-626d-43ff-b9a6-f39ad8f8b1e4

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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