FDA Inspection 1091122 - Anigan, Inc. - May 23, 2019

Record Details

This FDA Inspection record concerns Anigan, Inc., with an inspection on May 23, 2019, issued by the Center for Devices and Radiological Health, covering devices.

Company: Anigan, Inc.
Inspection Date: May 23, 2019
Product Type: Devices
Office: Center for Devices and Radiological Health

Open in Dashboard

ID · a469390e-1192-467e-a939-0c655308512f

Violation Codes2

21 CFR 820.30(f)21 CFR 820.30(g)

Full citation text and observation details available on the Dashboard.