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FDA Inspection
•Perma Pure LLC•March 6, 2026

Perma Pure LLC – FDA Inspection, Mar 6, 2026

Record Details

This FDA Inspection record concerns Perma Pure LLC, with an inspection on March 6, 2026, covering devices.

Company
Perma Pure LLC
Inspection Date
March 6, 2026
Product Type
Devices
Person
  • Shirley S. Wen (Issuing Officer)
View Company Profile

ID · c7b1b42c-28de-49d3-b73c-1a3714a1e061

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1309030
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

Other FDA inspections of Perma Pure LLC

6
DateClassificationOfficeProject area
January 3, 2020NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
January 21, 2016NAICenter for Devices and Radiological HealthCompliance: Devices
July 9, 2013VAICenter for Devices and Radiological HealthCompliance: Devices
September 19, 2011VAICenter for Devices and Radiological HealthCompliance: Devices
March 18, 2011OAICenter for Devices and Radiological HealthCompliance: Devices
View all 6 other inspections on the company page
Other documents for Perma Pure LLC
  • FDA Inspection 1115239 - 2020-01-03
  • FDA Inspection 956470 - 2016-01-21
  • FDA Inspection 838041 - 2013-07-09
  • FDA Inspection 745531 - 2011-09-19
  • FDA Inspection 713530 - 2011-03-18

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