FDA Inspection
Perma Pure LLCPerma Pure LLC – FDA Inspection, Mar 18, 2011
Record Details
This FDA Inspection record concerns Perma Pure LLC, with an inspection on March 18, 2011, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Perma Pure LLC
- Inspection Date
- March 18, 2011
- Product Type
- Devices
View Company Profile
ID · 9adcb502-564e-4e1e-a1c4-3c3887778439
Inspection Facts
Official Action Indicated (OAI)
Significant objectionable conditions were found and regulatory or administrative action is recommended.
- Inspection number
- 713530
- 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 |
| January 21, 2016 | NAI | Center for Devices and Radiological Health | Compliance: 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 |
Other documents for Perma Pure LLC
- FDA Inspection 1309030 - 2026-03-06
- FDA Inspection 1115239 - 2020-01-03
- FDA Inspection 956470 - 2016-01-21
- FDA Inspection 838041 - 2013-07-09
- FDA Inspection 745531 - 2011-09-19
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