# FDA Inspection 819002 - Amron International, Inc. - February 19, 2013

Source: https://www.globalkeysolutions.net/records/fda_inspections/amron-international-inc/bbe849ff-323c-4255-a351-8f43bc5eb59d
Source feed: FDA_Inspections

> FDA Inspection 819002 for Amron International, Inc. on February 19, 2013. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 819002
- Company Name: Amron International, Inc.
- Inspection Date: 2013-02-19
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1040716 - 2018-01-10](https://www.globalkeysolutions.net/records/fda_inspections/amron-international-inc/ab280b1f-2d18-4f27-85a8-a75c4107a0d5)
- [FDA Inspection 1040716 - 2018-01-10](https://www.globalkeysolutions.net/records/fda_inspections/amron-international-inc/f340998d-ff26-45bf-821b-6f89e2bdd14a)
- [FDA Inspection 819002 - 2013-02-19](https://www.globalkeysolutions.net/records/fda_inspections/amron-international-inc/3b1b7305-4ad1-447a-ad46-5cdb4c9f1239)

Company: https://www.globalkeysolutions.net/companies/amron-international-inc/11339df0-f236-416f-b7cd-c47c97410572

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