FDA Inspection 1074420 - Full Power AED LLC - December 14, 2018

FDA Inspection 1074420 for Full Power AED LLC on December 14, 2018. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1074420 for Full Power AED LLC on December 14, 2018. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 803.17

21 CFR 820.100(a)

21 CFR 820.198(a)

21 CFR 820.30(c)

21 CFR 820.30(d)

21 CFR 820.30(f)

21 CFR 820.30(g)

21 CFR 820.50(b)

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Record Information

Company

Full Power AED LLC

Inspection Date

December 14, 2018

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fceca7a0-1f74-4964-9ca9-c752b33c3ed5

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