FDA WARNING_LETTER - Lasik Laser - November 02, 2009

FDA WARNING_LETTER for Lasik Laser on November 02, 2009. Product: Devices. Access full analysis and detailed observations.

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Record Summary

FDA WARNING_LETTER for Lasik Laser on November 02, 2009. Product: Devices. Access full analysis and detailed observations.

Violation Codes

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

21 U.S.C. 321(h)

21 CFR 803

21 U.S.C. 360i

21 CFR 803.17

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Record Information

Company

Lasik Laser

Inspection Date

November 2, 2009

Product Type

Devices

Office

Center for Devices and Radiological Health

People

ID: 0a23051e-575a-4a57-b2d6-dc2fefaa419a

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