FDA WARNING_LETTER - ConMed Electrosurgery - September 20, 2013

FDA WARNING_LETTER for ConMed Electrosurgery on September 20, 2013. Product: Devices. Access full analysis and detailed observations.

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Record Summary

FDA WARNING_LETTER for ConMed Electrosurgery on September 20, 2013. Product: Devices. Access full analysis and detailed observations.

Violation Codes

21 U.S.C. 360j(g)

21 U.S.C. 352(t)(2)

21 U.S.C. 351(f)(1)(B)

21 CFR 820.100(a)

21 CFR 820.30(i)

21 CFR 820.70(c)

21 CFR 820

21 CFR 820.72(a)

21 U.S.C. 321(h)

21 U.S.C. 360(k)

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Record Information

Company

ConMed Electrosurgery

Inspection Date

September 20, 2013

Product Type

Devices

Office

Denver District Office

People

ID: ab3f58f3-973f-443a-b1b0-5d928eb543e7

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