FDA Inspection 1024384 - Ferndale Laboratories, Inc. - August 02, 2017

FDA Inspection 1024384 for Ferndale Laboratories, Inc. on August 02, 2017. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 1024384 for Ferndale Laboratories, Inc. on August 02, 2017. Classification: No Action Indicated (NAI).

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Record Information

Company

Ferndale Laboratories, Inc.

Inspection Date

August 2, 2017

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: 2047636e-acff-42ac-ba48-1c0bd26eb3fe

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