# FDA Inspection 993550 - VertiFlex, Inc. - July 19, 2016

Source: https://www.globalkeysolutions.net/records/fda_inspections/vertiflex-inc/fdf35d7a-fc36-4ed2-bc7e-506b38c4d27a/
Source feed: FDA_Inspections

> FDA Inspection 993550 for VertiFlex, Inc. on July 19, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 993550
- Company Name: VertiFlex, Inc.
- Inspection Date: 2016-07-19
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 993550 - 2016-07-19](https://www.globalkeysolutions.net/api/records/fda_inspections/vertiflex-inc/6108d677-efd7-463c-9701-55da1a8c017b/)
- [FDA Inspection 888763 - 2014-07-25](https://www.globalkeysolutions.net/api/records/fda_inspections/vertiflex-inc/f45711ea-f3cf-41c4-aef4-1e17591efd4a/)
- [FDA Inspection 881232 - 2014-05-16](https://www.globalkeysolutions.net/api/records/fda_inspections/vertiflex-inc/0fc851fd-5b43-4be2-abbd-e956677cd1fa/)
- [FDA Inspection 881232 - 2014-05-16](https://www.globalkeysolutions.net/api/records/fda_inspections/vertiflex-inc/e172625e-9fe1-4377-a43e-a2cde7806acc/)
- [FDA Inspection 647468 - 2010-02-11](https://www.globalkeysolutions.net/api/records/fda_inspections/vertiflex-inc/96b6012b-af16-4126-b274-1b7d383f1618/)

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