483 Acro Biotech May 2018

483 Acro Biotech May 2018

Sonya Karsik FDA$119.00 - Available Now

FDA investigators audited the Acro Biotech - Rancho Cucamonga, CA, United States facility and issued inspectional observations (via FDA 483) on 01 May 2018.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 01 May 2018
  • Location: Rancho Cucamonga, United States
  • FEI: 3005670738
Add To Cart