# FDA Inspection 938404 - Gentell, Inc - August 25, 2015

Source: https://www.globalkeysolutions.net/records/fda_inspections/gentell-inc/8f1ee047-7ab8-4eeb-95cf-268c0d8bb906
Source feed: FDA_Inspections

> FDA Inspection 938404 for Gentell, Inc on August 25, 2015. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 938404
- Company Name: Gentell, Inc
- Inspection Date: 2015-08-25
- Classification: Official Action Indicated (OAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/gentell-inc/96d27734-9ad8-46a1-9b0d-77fdcaaffb88

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