FDA Inspection 1028776 - MSK Precision Products, Inc. - March 21, 2017

FDA Inspection 1028776 for MSK Precision Products, Inc. on March 21, 2017. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1028776 for MSK Precision Products, Inc. on March 21, 2017. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 803.17

21 CFR 820.198(a)

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Record Information

Company

MSK Precision Products, Inc.

Inspection Date

March 21, 2017

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fd78473b-a9d4-467e-8aea-03349fbf975e

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