FDA Inspection 1024252 - Ajinomoto Althea, Inc. - April 06, 2017

FDA Inspection 1024252 for Ajinomoto Althea, Inc. on April 06, 2017. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1024252 for Ajinomoto Althea, Inc. on April 06, 2017. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 211.160(a)

21 CFR 211.67(b)

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Record Information

Company

Ajinomoto Althea, Inc.

Inspection Date

April 6, 2017

Product Type

Drugs

Office

Center for Drug Evaluation and Research

ID: 553d0093-11e5-4304-8a8a-d066a0fc9725

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