# FDA Inspection 1112957 - Gentell - December 16, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/gentell/8ea9ee83-44f4-475d-bd1c-f0f84976b861
Source feed: FDA_Inspections

> FDA Inspection 1112957 for Gentell on December 16, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1112957
- Company Name: Gentell
- Inspection Date: 2019-12-16
- 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/gentell/f1be9ee8-d5cd-48bb-b91d-ae8204bced09

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