FDA Inspection 1000722 - BIO LAB-ST. JOSEPH CORP - January 18, 2017

FDA Inspection 1000722 for BIO LAB-ST. JOSEPH CORP on January 18, 2017. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1000722 for BIO LAB-ST. JOSEPH CORP on January 18, 2017. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 820.100(a)

21 CFR 820.250(b)

21 CFR 820.50

21 CFR 820.70(a)

21 CFR 820.70(c)

21 CFR 820.75(a)

21 CFR 820.75(b)

21 CFR 820.80(d)

21 CFR 820.90(b)(1)

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Record Information

Company

BIO LAB-ST. JOSEPH CORP

Inspection Date

January 18, 2017

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: cbb68a6a-6918-472c-b02a-f9db21a55074

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