# FDA Inspection 595035 - Zimmer Spine, Inc. - July 09, 2009

Source: https://www.keypedia.com/records/fda_inspections/zimmer-spine-inc/10d420de-3e63-4771-a73e-e25d885d1028
Source feed: FDA_Inspections

> FDA Inspection 595035 for Zimmer Spine, Inc. on July 09, 2009. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 595035
- Company Name: Zimmer Spine, Inc.
- Inspection Date: 2009-07-09
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 832245 - 2013-05-10](https://www.keypedia.com/records/fda_inspections/zimmer-spine-inc/141a880c-2668-4029-8995-204c34f9ebb4)
- [FDA Inspection 648577 - 2010-02-25](https://www.keypedia.com/records/fda_inspections/zimmer-spine-inc/11a5d0df-9fa1-4c03-8c0d-6d84f0d3b510)
- [FDA Inspection 639639 - 2010-01-21](https://www.keypedia.com/records/fda_inspections/zimmer-spine-inc/8579d579-e8f5-48db-968f-6fb8977de8dc)

Company: https://www.keypedia.com/companies/zimmer-spine-inc/9cc28dba-16b8-4928-be98-889156173471

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