# FDA Inspection 630672 - Zimmer Spine, Inc. - November 06, 2009

Source: https://www.globalkeysolutions.net/records/fda_inspections/zimmer-spine-inc/3bcc2a98-2d07-4052-9406-1c72d0cd7a97
Source feed: FDA_Inspections

> FDA Inspection 630672 for Zimmer Spine, Inc. on November 06, 2009. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 630672
- Company Name: Zimmer Spine, Inc.
- Inspection Date: 2009-11-06
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 826674 - 2013-04-03](https://www.globalkeysolutions.net/records/fda_inspections/zimmer-spine-inc/74087401-0b70-4da0-b16a-b36a71ed7bf9)
- [FDA Inspection 630672 - 2009-11-06](https://www.globalkeysolutions.net/records/fda_inspections/zimmer-spine-inc/fca1ff08-2b86-4d9f-8984-4c23957dce29)

Company: https://www.globalkeysolutions.net/companies/zimmer-spine-inc/296dc303-a37c-410c-a93d-88643547b354

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