FDA EIR - Zhejiang Huahai Pharmaceutical - May 19, 2017

FDA EIR for Zhejiang Huahai Pharmaceutical on May 19, 2017. Product: Drugs. Access full analysis and detailed observations.

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Record Summary

FDA EIR for Zhejiang Huahai Pharmaceutical on May 19, 2017. Product: Drugs. Access full analysis and detailed observations.

Violation Codes

21 CFR 501(a)(2)(B)

21 CFR 211.192

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Record Information

Company

Zhejiang Huahai Pharmaceutical

Inspection Date

May 19, 2017

Product Type

Drugs

Office

CDER/OC

People

ID: 4f117789-6333-46f2-825b-833001cf712d

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