# FDA Inspection 605389 - Pacesetter Inc - July 29, 2009

Source: https://www.globalkeysolutions.net/records/fda_inspections/pacesetter-inc/f8558eeb-7bf0-4a63-885f-8c8927b87519/
Source feed: FDA_Inspections

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

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## Details

- Record Type: FDA Inspection
- Inspection ID: 605389
- Company Name: Pacesetter Inc
- Inspection Date: 2009-07-29
- Classification: Official Action Indicated (OAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/pacesetter-inc/c5dfe475-e9fc-4fe9-acdd-3c6f76e72626

Office: https://www.globalkeysolutions.net/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7