# FDA Inspection 1048839 - Anigan, Inc. - April 19, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/anigan-inc/d158e4a4-235f-485c-b3df-9275b10d2e22
Source feed: FDA_Inspections

> FDA Inspection 1048839 for Anigan, Inc. on April 19, 2018. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1048839
- Company Name: Anigan, Inc.
- Inspection Date: 2018-04-19
- Classification: Official Action Indicated (OAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1091122 - 2019-05-23](https://www.globalkeysolutions.net/records/fda_inspections/anigan-inc/a469390e-1192-467e-a939-0c655308512f)

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

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