FDA WARNING_LETTER - AES Optics - May 20, 2010

FDA WARNING_LETTER for AES Optics on May 20, 2010. Product: Devices. Access full analysis and detailed observations.

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Record Summary

FDA WARNING_LETTER for AES Optics on May 20, 2010. Product: Devices. Access full analysis and detailed observations.

Violation Codes

21 CFR 820.22

21 CFR 820.250(a)

21 CFR 820

21 CFR 820.70(a)(5)

21 CFR 820.100(b)

21 U.S.C. 351(h)

21 CFR 820.20(d)

21 CFR 803.17

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Record Information

Company

AES Optics

Inspection Date

May 20, 2010

Product Type

Devices

Office

New Orleans District Office

People

ID: 158b7b8c-9dfb-4bb4-bd7b-85357a143d3b

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