# Multigon Industries Inc – FDA Inspection, Sep 17, 2018

Source: https://www.keypedia.com/records/fda_inspections/multigon-industries-inc/347f0d6c-2f5d-4bc3-a3d0-7813c12c98b9
Source feed: FDA_Inspections

> FDA inspection 1065931 of Multigon Industries Inc, September 17, 2018. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 820. Form 483 issued. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1065931
- Company Name: Multigon Industries Inc
- Inspection Date: 2018-09-17
- 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 1163355 - 2022-02-25
- FDA Inspection 921550 - 2015-03-27
- FDA Inspection 812052 - 2012-12-18
- FDA Inspection 704663 - 2010-12-09

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/jacqueline-s-warner/d001f4ec-db46-4d78-a5dd-efea7ddfb893)

Company: https://www.keypedia.com/companies/multigon-industries-inc/e6cefdb3-72ec-413c-a6e4-cf7d2050818d

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