FDA Inspection 1210950 - Aurobindo Pharma Ltd - July 21, 2023

FDA Inspection 1210950 for Aurobindo Pharma Ltd on July 21, 2023. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1210950 for Aurobindo Pharma Ltd on July 21, 2023. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 211.160(a)

21 CFR 211.56(a)

21 CFR 211.67(b)

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Record Information

Company

Aurobindo Pharma Ltd

Inspection Date

July 21, 2023

Product Type

Drugs

Office

Center for Drug Evaluation and Research

ID: 456ed1f7-cbc3-4ed8-a484-85c4b018e2fa

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