# American IV Products, Inc. – FDA Inspection, Sep 12, 2018

Source: https://www.keypedia.com/records/fda_inspections/american-iv-products-inc/dc15810b-044b-4c64-a3a3-c60db2fcdc99
Source feed: FDA_Inspections

> FDA inspection 1066151 of American IV Products, Inc., September 12, 2018. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 820. Form 483 issued. 5 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1066151
- Company Name: American IV Products, Inc.
- Inspection Date: 2018-09-12
- 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: 4

## Related Documents

- [FDA Inspection 1246121 - 2024-08-12](https://www.keypedia.com/records/fda_inspections/american-iv-products-inc/d23e8a61-0f06-4b37-b6df-48a670904b62)
- [FDA Inspection 987959 - 2016-10-19](https://www.keypedia.com/records/fda_inspections/american-iv-products-inc/9bba9c61-2431-4961-aaf8-60a049848669)
- FDA Inspection 874152 - 2014-04-09
- FDA Inspection 734086 - 2011-07-27
- FDA Inspection 672266 - 2010-07-21

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/jacob-m-dyer/e3ca27e3-e0b1-4db8-9cbe-cfaff90b83cf)

Company: https://www.keypedia.com/companies/american-iv-products-inc/d45ab8ed-d031-4d23-bf91-ddb16bac4e93

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