# VertiFlex, Inc. – FDA Inspection, Jul 25, 2014

Source: https://www.keypedia.com/records/fda_inspections/vertiflex-inc/f45711ea-f3cf-41c4-aef4-1e17591efd4a
Source feed: FDA_Inspections

> FDA inspection 888763 of VertiFlex, Inc., July 25, 2014. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 812. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 888763
- Company Name: VertiFlex, Inc.
- Inspection Date: 2014-07-25
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

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- FDA Inspection 881232 - 2014-05-16
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- [FDA Inspection 541038 - 2008-10-07](https://www.keypedia.com/records/fda_inspections/vertiflex-inc/ebec3bb6-cee9-4e2d-b3b2-2aade388d36c)

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