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483 Acro Biotech, May 2018

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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
Acro Biotech FDA inspection 483 May 2018