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FDA Inspection 981282 — MPP PHARMA LLC

MPP PHARMA LLC — FEI 1930436

The FDA completed an inspection of MPP PHARMA LLC on April 4, 2016 in Kansas City, MO. 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
April 4, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Kansas City, MO (United States)

Facility

Other inspections at this facility

  • 1310538 (OAI Thu Apr 02 2026 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1239037 (VAI Fri Sep 20 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1250844 (VAI Fri Sep 13 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1140517 (VAI Wed Apr 21 2021 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 867588 (VAI Wed Feb 19 2014 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources