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FDA Inspection 1215954 — AML Riverside, LLC

AML Riverside, LLC — FEI 1931411

The FDA completed an inspection of AML Riverside, LLC on August 18, 2023 in Fort Dodge, IA. 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 18, 2023
Fiscal Year
2023
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Fort Dodge, IA (United States)

Facility

Other inspections at this facility

  • 1084908 (VAI Wed Apr 03 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1038531 (NAI Thu Jan 18 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 968477 (NAI Thu May 05 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 818763 (NAI Fri Feb 15 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 707897 (NAI Fri Jan 21 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources