FDA Inspection 871900 - 3M Unitek Corporation - March 27, 2014

FDA Inspection 871900 for 3M Unitek Corporation on March 27, 2014. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 871900 for 3M Unitek Corporation on March 27, 2014. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 803.50(a)(1)

21 CFR 820.25(b)

21 CFR 820.30(c)

21 CFR 820.30(e)

21 CFR 820.30(i)

21 CFR 820.40(b)

21 CFR 820.72(b)

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Record Information

Company

3M Unitek Corporation

Inspection Date

March 27, 2014

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f9a2c034-a20c-4a46-b4b7-7bb83aa86692

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