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FDA Inspection 1199735 — Hemostasis, LLC

Hemostasis, LLC — FEI 3007225047

The FDA completed an inspection of Hemostasis, LLC on February 3, 2023 in Saint Paul, MN. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
February 3, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Saint Paul, MN (United States)

Facility

Other inspections at this facility

  • 1095951 (NAI Thu May 16 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 909852 (NAI Tue Jan 13 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 737542 (NAI Fri Jul 29 2011 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 559441 (VAI Mon Nov 17 2008 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources