FDA WARNING_LETTER - arrowhead de llc, - February 21, 2012

FDA WARNING_LETTER for arrowhead de llc, on February 21, 2012. Product: Devices. Access full analysis and detailed observations.

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Record Summary

FDA WARNING_LETTER for arrowhead de llc, on February 21, 2012. Product: Devices. Access full analysis and detailed observations.

Violation Codes

21 CFR 820.80(d)

21 CFR 820.30(h)

21 CFR 820.30(a)

21 CFR 820.198

21 CFR 820.100(a)

21 CFR 820.30(i)

21 CFR 820

21 U.S.C. 321(h)

21 CFR 820.100(a)(1)

21 CFR 820.100(a)(4)

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Record Information

Company

arrowhead de llc,

Inspection Date

February 21, 2012

Product Type

Devices

Office

New Orleans District Office

People

Patricia K. Schafer

ID: adc24881-b21c-48d9-81da-7a59a067bd4e

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