FDA Inspection 602130 - Steripac - July 30, 2009

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Record Details

This FDA Inspection record concerns Steripac, with an inspection on July 30, 2009, issued by the Center for Devices and Radiological Health, covering devices.

Company: Steripac
Inspection Date: July 30, 2009
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 4fe9b308-bcc5-4fbb-89f1-97e1c5f3aaa7

Violation Codes10

21 CFR 803.50(a)(2)21 CFR 820.100(b)21 CFR 820.181(b)21 CFR 820.18421 CFR 820.198(a)(3)21 CFR 820.20(c)21 CFR 820.2221 CFR 820.4021 CFR 820.5021 CFR 820.80(e)

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