# Integron Inc. – FDA Inspection, Dec 10, 2018

Source: https://www.keypedia.com/records/fda_inspections/integron-inc/29821645-90e1-4958-b9b1-697f9cfc2f46
Source feed: FDA_Inspections

> FDA inspection 1074303 of Integron Inc., December 10, 2018. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1074303
- Company Name: Integron Inc.
- Inspection Date: 2018-12-10
- 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: 1

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/joel-r-powers/b1c3a33f-1337-45ee-845a-e90688b8875a)
- [Issuing Officer](https://www.keypedia.com/people/matthew-d-schnittker/cf76f07f-db6d-47a0-8412-7eb084d4fe8b)

Company: https://www.keypedia.com/companies/integron-inc/1abca04a-c75c-4e67-b07e-064f737e1bbb

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