FDA Inspection 1015605 — Pentair Filtration Solutions, LLC

Pentair Filtration Solutions, LLC — FEI 1000221012

The FDA completed an inspection of Pentair Filtration Solutions, LLC on April 25, 2017 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 25, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Saint Paul, MN (United States)