# Henry Okonkwo, P.A. – FDA Inspection, Jul 1, 2018

Source: https://www.keypedia.com/records/fda_inspections/henry-okonkwo-pa/e3a2e246-1958-49a0-81e5-a41612b9b374
Source feed: FDA_Inspections

> FDA inspection 1058579 of Henry Okonkwo, P.A., July 01, 2018. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 812. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1058579
- Company Name: Henry Okonkwo, P.A.
- Inspection Date: 2018-07-01
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Project Evaluation: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Officers

- [Company Rep](https://www.keypedia.com/people/travis-m-beard/a89f6d0b-dc5b-4adc-84f5-36e04b00fc2d)

Company: https://www.keypedia.com/companies/henry-okonkwo-pa/a0d93495-dcfe-4be1-8c2b-03e46e3f0adb

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