# FDA Inspection 615341 - Depuy Spine Inc - September 25, 2009

Source: https://www.keypedia.com/records/fda_inspections/depuy-spine-inc/7ff3bf93-1ccd-4c1f-a965-ed23bfda16fc
Source feed: FDA_Inspections

> FDA Inspection 615341 for Depuy Spine Inc on September 25, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 615341
- Company Name: Depuy Spine Inc
- Inspection Date: 2009-09-25
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 770881 - 2012-03-06](https://www.keypedia.com/records/fda_inspections/depuy-spine-inc/40a8458b-0645-48cb-a3d4-a7f06efe980b)
- [FDA Inspection 770881 - 2012-03-06](https://www.keypedia.com/records/fda_inspections/depuy-spine-inc/0f83240d-897d-45cf-835b-4b28f87b660c)
- [FDA Inspection 615341 - 2009-09-25](https://www.keypedia.com/records/fda_inspections/depuy-spine-inc/914c0bc1-ed48-455b-a01a-9ba0027ec527)

Company: https://www.keypedia.com/companies/depuy-spine-inc/0f372fb1-22c0-4498-ba32-0bae36930b0e

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