FDA Inspection 823425 — Pentair Filtration Solutions, LLC

Pentair Filtration Solutions, LLC — FEI 1000221012

The FDA completed an inspection of Pentair Filtration Solutions, LLC on February 14, 2013 in Saint Paul, MN. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 5 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
February 14, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Saint Paul, MN (United States)

Citations

IDCFRDescription
313021 CFR 820.100(a)Lack of or inadequate procedures
319021 CFR 820.30(g)Design validation acceptance criteria
328621 CFR 820.90(b)(1)Procedures for product review,disposition lack of/inadequate
366621 CFR 820.20(c)Management review - Lack of or inadequate procedures
53921 CFR 820.70(b)Production and Process Change Procedures, lack of or Inad.