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

Biologics

Office

Center for Biologics Evaluation and Research

ID: 5f4ad951-3983-4065-a6a1-3056bae2a886

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