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FDA Inspection 678308 — Aurorium LLC

Aurorium LLC — FEI 1824624

The FDA completed an inspection of Aurorium LLC on August 27, 2010 in Zeeland, MI. 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 27, 2010
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Zeeland, MI (United States)

Facility

Other inspections at this facility

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  • 1206275 (NAI Thu May 11 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1085792 (VAI Tue Apr 09 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1002043 (NAI Tue Feb 28 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 887005 (VAI Fri Jul 11 2014 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources