FDA Inspection 614651 - CAPTEK, Inc. - September 25, 2009

FDA Inspection 614651 for CAPTEK, Inc. on September 25, 2009. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 614651 for CAPTEK, Inc. on September 25, 2009. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 820.184

21 CFR 820.20(a)

21 CFR 820.30(i)

21 CFR 820.30(j)

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Record Information

Company

CAPTEK, Inc.

Inspection Date

September 25, 2009

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f65c1aa4-280c-439e-bd3e-54014dc18708

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