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FDA Inspection 1171910 — Biomedix Wai

Biomedix Wai — FEI 1000115518

The FDA completed an inspection of Biomedix Wai on June 3, 2022 in Chanhassen, MN. 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
June 3, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Compliance: Devices
Location
Chanhassen, MN (United States)

Facility

Other inspections at this facility

  • 1255255 (NAI Mon Nov 18 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1110467 (NAI Thu Oct 31 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1056265 (VAI Fri Jun 08 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 952092 (VAI Wed Dec 09 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 821884 (OAI Mon Mar 04 2013 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources