FDA inspection
Pentair Filtration Solutions, LLC: FDA inspection ending Apr 25, 2017
FDA inspection 1015605 · No Action Indicated (NAI) · Saint Paul, MN
Key facts
| Inspection ID | 1015605 |
|---|---|
| Firm | Pentair Filtration Solutions, LLC |
| FEI number | 1000221012 |
| Address | 1350 Hammond Rd |
| City | Saint Paul |
| State | MN |
| ZIP | 55110 |
| Country | United States |
| Fiscal year | 2017 |
| Inspection end date | Apr 25, 2017 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No Form FDA 483 issued
- No Establishment inspection report (EIR) exists
- 1–9 Inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA inspections
FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.
Source: U.S. Food and Drug Administration (FDA), inspection classification data