FDA Inspection 830220 - Haemonetics Corporation - May 03, 2013

FDA Inspection 830220 for Haemonetics Corporation on May 03, 2013. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 830220 for Haemonetics Corporation on May 03, 2013. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 820.70(c)

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Record Information

Company

Haemonetics Corporation

Inspection Date

May 3, 2013

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fe17a70c-13c1-454d-b3c4-842242fcf3b1

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