FDA Inspection
Perma Pure LLCPerma Pure LLC – FDA Inspection, Sep 19, 2011
Record Details
This FDA Inspection record concerns Perma Pure LLC, with an inspection on September 19, 2011, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Perma Pure LLC
- Inspection Date
- September 19, 2011
- Product Type
- Devices
View Company Profile
ID · e70123dc-27fd-49ec-9873-028ac8913f5f
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 745531
- 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 |
| 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 956470 - 2016-01-21
- FDA Inspection 838041 - 2013-07-09
- FDA Inspection 713530 - 2011-03-18
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