Home / Inspections / 1049629

FDA Inspection 1049629 — ADMA Biologics, Inc

ADMA Biologics, Inc — FEI 1000525461

The FDA completed an inspection of ADMA Biologics, Inc on April 12, 2018 in Boca Raton, FL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
April 12, 2018
Fiscal Year
2018
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Boca Raton, FL (United States)

Facility

Other inspections at this facility

  • 1256275 (VAI Wed Dec 11 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1219342 (NAI Wed Sep 20 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1150114 (VAI Thu Aug 12 2021 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 974061 (OAI Thu Mar 03 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 892829 (OAI Thu Aug 14 2014 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources