FDA issued a Warning Letter to Anigan, Inc. on 7/25/2018 as a result of this inspection.
FDA investigators audited the Anigan - San Ramon, CA, United States facility and issued inspectional observations (via FDA 483) on 19 Apr 2018.
Product details
- Category: Medical Devices & Rad Health
- Inspection end: 19 Apr 2018
- Location: San Ramon, United States
- FEI: 3009666823
