# FDA Inspection 980582 - Ameriflo2 Incorporated - March 25, 2016

Source: https://www.keypedia.com/records/fda_inspections/ameriflo2-incorporated/15cac407-9872-4c7b-ad36-36c28c4720db
Source feed: FDA_Inspections

> FDA Inspection 980582 for Ameriflo2 Incorporated on March 25, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 980582
- Company Name: Ameriflo2 Incorporated
- Inspection Date: 2016-03-25
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 827711 - 2013-04-16](https://www.keypedia.com/records/fda_inspections/ameriflo2-incorporated/2a6b7ef1-d8b4-40a1-aa31-e865fa9f4803)
- [FDA Inspection 726538 - 2011-05-06](https://www.keypedia.com/records/fda_inspections/ameriflo2-incorporated/959e710e-f396-44da-a930-63712f8922ee)

Company: https://www.keypedia.com/companies/ameriflo2-incorporated/401e64ad-23c0-44cf-92db-79bc86d1c8c2

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