FDA Inspection 818223 - Continental Medical Labs, Inc. - February 08, 2013

FDA Inspection 818223 for Continental Medical Labs, Inc. on February 08, 2013. Classification: Official Action Indicated (OAI).

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Record Summary

FDA Inspection 818223 for Continental Medical Labs, Inc. on February 08, 2013. Classification: Official Action Indicated (OAI).

Violation Codes

21 CFR 803.17

21 CFR 820.100(a)

21 CFR 820.198(a)

21 CFR 820.20(c)

21 CFR 820.70(c)

21 CFR 820.75(a)

21 CFR 820.90(a)

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Record Information

Company

Continental Medical Labs, Inc.

Inspection Date

February 8, 2013

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: 70963b68-b5f8-45b6-8054-082b18441727

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