FDA Inspection 1080798 - Patheon Softgels Inc. - January 30, 2019

FDA Inspection 1080798 for Patheon Softgels Inc. on January 30, 2019. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 1080798 for Patheon Softgels Inc. on January 30, 2019. Classification: No Action Indicated (NAI).

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Record Information

Company

Patheon Softgels Inc.

Inspection Date

January 30, 2019

Product Type

Drugs

Office

Center for Drug Evaluation and Research

ID: 7d15b8cd-5597-4a83-adf4-0ebe8dc4994c

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