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FDA Inspection 1147150 — Katecho LLC

Katecho LLC — FEI 1930027

The FDA completed an inspection of Katecho LLC on July 16, 2021 in Des Moines, IA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
July 16, 2021
Fiscal Year
2021
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Des Moines, IA (United States)

Facility

Other inspections at this facility

  • 1229069 (NAI Thu Aug 01 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1181164 (NAI Thu Sep 15 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1040498 (NAI Wed Dec 06 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1034156 (VAI Fri Mar 31 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 871935 (NAI Fri Mar 28 2014 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources