# FDA Inspection 544331 - Amrex Zetron Inc - November 03, 2008

Source: https://www.globalkeysolutions.net/records/fda_inspections/amrex-zetron-inc/f2d4bfa8-89e6-4c43-a372-c659e8cfda35
Source feed: FDA_Inspections

> FDA Inspection 544331 for Amrex Zetron Inc on November 03, 2008. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 544331
- Company Name: Amrex Zetron Inc
- Inspection Date: 2008-11-03
- Classification: Official Action Indicated (OAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/amrex-zetron-inc/9ffedd93-a4aa-4b3e-bee6-d6e7221f577d

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