FDA Inspection 1074273 - Mpi Medical Products, Inc. - December 04, 2018

FDA Inspection 1074273 for Mpi Medical Products, Inc. on December 04, 2018. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1074273 for Mpi Medical Products, Inc. on December 04, 2018. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 803.17

21 CFR 820.100(a)

21 CFR 820.184

21 CFR 820.22

21 CFR 820.30(i)

21 CFR 820.50

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Record Information

Company

Mpi Medical Products, Inc.

Inspection Date

December 4, 2018

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: 85730521-cb15-4ed4-980f-ef8a378a9e8b

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