# iScreen Vision, Inc. – FDA Inspection, Sep 28, 2023

Source: https://www.keypedia.com/records/fda_inspections/iscreen-vision-inc/da267491-7a64-4f24-be91-d14e321a99b3
Source feed: FDA_Inspections

> FDA inspection 1219047 of iScreen Vision, Inc., September 28, 2023. Classification: Voluntary Action Indicated (VAI). 5 citations under 21 CFR part 820. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1219047
- Company Name: iScreen Vision, Inc.
- Inspection Date: 2023-09-28
- 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 911600 - 2015-01-28
- FDA Inspection 760707 - 2011-12-21
- FDA Inspection 551252 - 2008-12-02

## Related Officers

- [Mary A. Millner](https://www.keypedia.com/people/mary-a-millner/bd8911cf-849d-41d2-ae12-dd4bad66e798)

Company: https://www.keypedia.com/companies/iscreen-vision-inc/bbe23b01-c949-404d-a86c-44a909c7d8b4

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