FDA Inspection 1018436 - Ajinomoto Althea, Inc. - June 01, 2017

FDA Inspection 1018436 for Ajinomoto Althea, Inc. on June 01, 2017. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1018436 for Ajinomoto Althea, Inc. on June 01, 2017. Classification: Voluntary Action Indicated (VAI).

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Record Information

Company

Ajinomoto Althea, Inc.

Inspection Date

June 1, 2017

Product Type

Biologics

Office

Center for Biologics Evaluation and Research

ID: cd2a50b5-f70e-4f8c-bf96-eb2d86b96833

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