FDA Inspection 1096784 - Anacom General Corporation DBA Anacom MedTek - July 12, 2019

FDA Inspection 1096784 for Anacom General Corporation DBA Anacom MedTek on July 12, 2019. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1096784 for Anacom General Corporation DBA Anacom MedTek on July 12, 2019. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 803.17

21 CFR 820.100(a)

21 CFR 820.184

21 CFR 820.198(a)

21 CFR 820.25(b)

21 CFR 820.50

21 CFR 820.80(b)

21 CFR 820.80(d)

21 CFR 820.90(a)

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Record Information

Company

Anacom General Corporation DBA Anacom MedTek

Inspection Date

July 12, 2019

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f87c6f2f-ec6c-4aa6-8aa8-fbb7a8de54f0

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