FDA Inspection 1023652 - Patheon Softgels Inc. - August 11, 2017

FDA Inspection 1023652 for Patheon Softgels Inc. on August 11, 2017. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 1023652 for Patheon Softgels Inc. on August 11, 2017. Classification: No Action Indicated (NAI).

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Record Information

Company

Patheon Softgels Inc.

Inspection Date

August 11, 2017

Product Type

Drugs

Office

Center for Drug Evaluation and Research

ID: b8cdb143-dc59-4867-8c59-399a58e1d4bf

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