FDA WARNING_LETTER - Dr. Joel Kaplan Inc. - July 17, 2013

FDA WARNING_LETTER for Dr. Joel Kaplan Inc. on July 17, 2013. Product: Devices. Access full analysis and detailed observations.

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Record Summary

FDA WARNING_LETTER for Dr. Joel Kaplan Inc. on July 17, 2013. Product: Devices. Access full analysis and detailed observations.

Violation Codes

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

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

21 CFR 884.5970

21 CFR 820

21 U.S.C. 321(h)

21 U.S.C. 360(k)

21 U.S.C. 360e(a)

21 CFR 820.198(a)

21 CFR 807.81(a)(3)(ii)

21 CFR 807.81(b)

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Record Information

Company

Dr. Joel Kaplan Inc.

Inspection Date

July 17, 2013

Product Type

Devices

Office

Los Angeles District Office

People

ID: a4ff8472-309f-4017-868d-ffd3f515db4e

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