FDA WARNING_LETTER - Kayline Inc. - June 03, 2008

FDA WARNING_LETTER for Kayline Inc. on June 03, 2008. Product: Devices. Access full analysis and detailed observations.

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Record Summary

FDA WARNING_LETTER for Kayline Inc. on June 03, 2008. Product: Devices. Access full analysis and detailed observations.

Violation Codes

21 CFR 820.22

21 CFR 820.50(a)(1)

21 U.S.C. 321

21 CFR 820.50(a)(2)

21 CFR 820

21 CFR 820.100(a)(1)

21 CFR 820.80(b)

21 CFR 820.90(a)

21 CFR 820.100(a)(2)

21 CFR 820.80(a)

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Record Information

Company

Kayline Inc.

Inspection Date

June 3, 2008

Product Type

Devices

Office

New Orleans District Office

People

Tyler Thornburg (H.)

ID: 6c425a11-96aa-458c-984b-02fe1edb7dce

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