FDA issued a Warning Letter to Anigan, Inc. on 7/25/2018 for a previous inspection.
483 Anigan May 2019

483 Anigan May 2019

Sonya Karsik FDA$119.00 - Available Now

FDA investigators audited the Anigan - San Ramon, CA, United States facility and issued inspectional observations (via FDA 483) on 23 May 2019.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 23 May 2019
  • Location: San Ramon, United States
  • FEI: 3009666823
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