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FDA Inspection 1008491 — Lifecore Biomedical, LLC

Lifecore Biomedical, LLC — FEI 1000115753

The FDA completed an inspection of Lifecore Biomedical, LLC on February 22, 2017 in Chaska, MN. 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
February 22, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Chaska, MN (United States)

Facility

Other inspections at this facility

  • 1252478 (VAI Wed Mar 12 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1082292 (VAI Tue Feb 26 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 954610 (VAI Fri Nov 20 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 830835 (NAI Thu Apr 25 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 768986 (NAI Fri Feb 24 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources