FDA Inspection
Perma Pure LLCPerma Pure LLC – FDA Inspection, Jan 21, 2016
Record Details
This FDA Inspection record concerns Perma Pure LLC, with an inspection on January 21, 2016, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Perma Pure LLC
- Inspection Date
- January 21, 2016
- Product Type
- Devices
View Company Profile
ID · 1f1feebf-bc7a-4e1f-95cd-7136b9f5bb4a
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 956470
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of Perma Pure LLC
6| Date | Classification | Office | Project area |
|---|---|---|---|
| March 6, 2026 | NAI | Compliance: Devices | |
| January 3, 2020 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| July 9, 2013 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| September 19, 2011 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| March 18, 2011 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Perma Pure LLC
- FDA Inspection 1309030 - 2026-03-06
- FDA Inspection 1115239 - 2020-01-03
- FDA Inspection 838041 - 2013-07-09
- FDA Inspection 745531 - 2011-09-19
- FDA Inspection 713530 - 2011-03-18
Document or profile
One record shows the event. A profile shows the pattern.
Buy this document for the source file and details behind this single event.
Choose full profile access to connect related records, sites, people, citations, and enforcement history in one view.