# Ameriflo2 Incorporated – FDA Inspection, Apr 16, 2013

Source: https://www.keypedia.com/records/fda_inspections/ameriflo2-incorporated/2a6b7ef1-d8b4-40a1-aa31-e865fa9f4803
Source feed: FDA_Inspections

> FDA inspection 827711 of Ameriflo2 Incorporated, April 16, 2013. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR parts 803 and 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 827711
- Company Name: Ameriflo2 Incorporated
- Inspection Date: 2013-04-16
- 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: 2

## Related Documents

- [FDA Inspection 980582 - 2016-03-25](https://www.keypedia.com/records/fda_inspections/ameriflo2-incorporated/15cac407-9872-4c7b-ad36-36c28c4720db)
- FDA Inspection 726538 - 2011-05-06

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