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FDA Inspection 979363 — AURORIUM LLC

AURORIUM LLC — FEI 1628757

The FDA completed an inspection of AURORIUM LLC on August 5, 2016 in Midlothian, TX. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
August 5, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Midlothian, TX (United States)

Facility

Other inspections at this facility

  • 1306572 (VAI Fri Mar 06 2026 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1053761 (VAI Mon May 14 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 811550 (NAI Thu Dec 20 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 665184 (NAI Mon Jun 07 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources