# FDA Inspection 1092360 - ApiFix, Ltd. - June 06, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/apifix-ltd/016f11a4-3325-4a70-956b-7f1001b65584
Source feed: FDA_Inspections

> FDA Inspection 1092360 for ApiFix, Ltd. on June 06, 2019. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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

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