FDA Inspection 1029560 - Eurofins Lancaster Laboratories, Inc - September 28, 2017

FDA Inspection 1029560 for Eurofins Lancaster Laboratories, Inc on September 28, 2017. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 1029560 for Eurofins Lancaster Laboratories, Inc on September 28, 2017. Classification: No Action Indicated (NAI).

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Record Information

Company

Eurofins Lancaster Laboratories, Inc

Inspection Date

September 28, 2017

Product Type

Drugs

Office

Center for Drug Evaluation and Research

ID: 9c3f7357-47cf-45d3-a8b8-4e318d5d223b

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