FDA Inspection 609551 - Abbott - August 20, 2009

FDA Inspection 609551 for Abbott on August 20, 2009. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 609551 for Abbott on August 20, 2009. Classification: No Action Indicated (NAI).

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Record Information

Company

Abbott

Inspection Date

August 20, 2009

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f7fe8418-17fb-4e8e-828f-3439b8f7e65d

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