FDA Inspection 605389 - Pacesetter Inc - July 29, 2009

FDA Inspection 605389 for Pacesetter Inc on July 29, 2009. Classification: Official Action Indicated (OAI).

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Record Summary

FDA Inspection 605389 for Pacesetter Inc on July 29, 2009. Classification: Official Action Indicated (OAI).

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Record Information

Company

Pacesetter Inc

Inspection Date

July 29, 2009

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f8558eeb-7bf0-4a63-885f-8c8927b87519

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