FDA issued a Warning Letter to Anigan, Inc. on 7/25/2018 as a result of this inspection.
483 Anigan Apr 2018

483 Anigan Apr 2018

Sara Richardson FDA$119.00 - Available Now

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
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