# Amrex Zetron Inc – FDA Inspection, Feb 8, 2024

Source: https://www.keypedia.com/records/fda_inspections/amrex-zetron-inc/6cf920ae-d872-49cb-84fd-cae04eac9010
Source feed: FDA_Inspections

> FDA inspection 1230398 of Amrex Zetron Inc, February 08, 2024. Classification: Voluntary Action Indicated (VAI). 5 citations under 21 CFR parts 801, 820 and 830. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1230398
- Company Name: Amrex Zetron Inc
- Inspection Date: 2024-02-08
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 5

## Related Documents

- [FDA Inspection 1040787 - 2018-01-17](https://www.keypedia.com/records/fda_inspections/amrex-zetron-inc/8378aa97-c1eb-45d8-bcff-22de3992097a)
- FDA Inspection 652380 - 2010-03-16
- [FDA Inspection 544331 - 2008-11-03](https://www.keypedia.com/records/fda_inspections/amrex-zetron-inc/f2d4bfa8-89e6-4c43-a372-c659e8cfda35)

## Related Officers

- [Company Rep](https://www.keypedia.com/people/juanita-banuelos/b8b581ef-b9f3-4d77-a9fa-691223dbb7f4)

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

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