FDA Inspection 828941 - Huestis Machine Corporation - May 13, 2013

FDA Inspection 828941 for Huestis Machine Corporation on May 13, 2013. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 828941 for Huestis Machine Corporation on May 13, 2013. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 1002.13

21 CFR 1002.41(a)(1)

21 CFR 820.181

21 CFR 820.184

21 CFR 820.198(a)

21 CFR 820.22

21 CFR 820.70(f)

21 CFR 820.75(a)

21 CFR 820.80(e)

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Record Information

Company

Huestis Machine Corporation

Inspection Date

May 13, 2013

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f96645c7-539a-497a-9a6c-9122e45b7c3f

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