FDA Inspection 971979 - Eurofins BioPharma Product Testing ENCO Inc. - May 04, 2016

FDA Inspection 971979 for Eurofins BioPharma Product Testing ENCO Inc. on May 04, 2016. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 971979 for Eurofins BioPharma Product Testing ENCO Inc. on May 04, 2016. Classification: No Action Indicated (NAI).

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Record Information

Company

Eurofins BioPharma Product Testing ENCO Inc.

Inspection Date

May 4, 2016

Product Type

Drugs

Office

Center for Drug Evaluation and Research

ID: f8381081-fa21-43d5-9e80-8b9e99241713

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