# VertiFlex, Inc. – FDA Inspection, Feb 11, 2010

Source: https://www.keypedia.com/records/fda_inspections/vertiflex-inc/96b6012b-af16-4126-b274-1b7d383f1618
Source feed: FDA_Inspections

> FDA inspection 647468 of VertiFlex, Inc., February 11, 2010. Classification: Official Action Indicated (OAI). 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 647468
- Company Name: VertiFlex, Inc.
- Inspection Date: 2010-02-11
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

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- [FDA Inspection 888763 - 2014-07-25](https://www.keypedia.com/records/fda_inspections/vertiflex-inc/f45711ea-f3cf-41c4-aef4-1e17591efd4a)
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Company: https://www.keypedia.com/companies/vertiflex-inc/3bf3ef7e-e14e-4bbc-9cd8-d9c99669b230

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