# FDA Inspection 541038 - VertiFlex, Inc. - October 07, 2008

Source: https://www.globalkeysolutions.net/records/fda_inspections/vertiflex-inc/d2bbe648-2ed2-4cec-b912-2fb896e3bedf
Source feed: FDA_Inspections

> FDA Inspection 541038 for VertiFlex, Inc. on October 07, 2008. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 541038
- Company Name: VertiFlex, Inc.
- Inspection Date: 2008-10-07
- Classification: Voluntary Action Indicated (VAI)
- 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/vertiflex-inc/3bf3ef7e-e14e-4bbc-9cd8-d9c99669b230

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