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FDA Inspection 1288354 — Morton Salt, Inc.

Morton Salt, Inc. — FEI 1910448

The FDA completed an inspection of Morton Salt, Inc. on November 6, 2025 in South Hutchinson, KS. 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
November 6, 2025
Fiscal Year
2026
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
South Hutchinson, KS (United States)

Facility

Other inspections at this facility

  • 1228627 (NAI Wed Jan 10 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1139966 (VAI Thu Apr 01 2021 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1041779 (NAI Tue Feb 13 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1042266 (VAI Thu Feb 08 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 912470 (VAI Thu Jan 29 2015 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources