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FDA Inspection 1167939 — Pentair Filtration Solutions, LLC

Pentair Filtration Solutions, LLC — FEI 1000221012

The FDA completed an inspection of Pentair Filtration Solutions, LLC on April 12, 2022 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
April 12, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Compliance: Devices
Location
Saint Paul, MN (United States)

Facility

Other inspections at this facility

  • 1015605 (NAI Tue Apr 25 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 823425 (NAI Thu Feb 14 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 674775 (NAI Thu Jul 15 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources