# Anigan, Inc. – FDA Inspection, May 23, 2019

Source: https://www.keypedia.com/records/fda_inspections/anigan-inc/a469390e-1192-467e-a939-0c655308512f
Source feed: FDA_Inspections

> FDA inspection 1091122 of Anigan, Inc., May 23, 2019. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1091122
- Company Name: Anigan, Inc.
- Inspection Date: 2019-05-23
- 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 1080171 - 2019-01-31
- [FDA Inspection 1048839 - 2018-04-19](https://www.keypedia.com/records/fda_inspections/anigan-inc/d158e4a4-235f-485c-b3df-9275b10d2e22)

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/sonya-l-karsik/c24603b9-5ca0-46f5-861a-b367155b0def)

Company: https://www.keypedia.com/companies/anigan-inc/f61a5fd3-5587-4f3b-a914-47e4f488e5e3

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