# ApiFix, Ltd. – FDA Inspection, Jun 6, 2019

Source: https://www.keypedia.com/records/fda_inspections/apifix-ltd/eaeebd11-0f20-4813-9596-517fb7ee156a
Source feed: FDA_Inspections

> FDA inspection 1092360 of ApiFix, Ltd., June 06, 2019. Classification: Voluntary Action Indicated (VAI). 6 citations under 21 CFR part 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1092360
- Company Name: ApiFix, Ltd.
- Inspection Date: 2019-06-06
- 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: 6

## Related Officers

- [Company Rep](https://www.keypedia.com/people/maida-henesian/cd28e878-000c-4af8-8dbd-4863057758bb)
- [Mary A. Millner](https://www.keypedia.com/people/mary-a-millner/bd8911cf-849d-41d2-ae12-dd4bad66e798)

Company: https://www.keypedia.com/companies/apifix-ltd/a35c688f-6f82-4168-95bd-811b16763d78

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