# Perma Pure LLC – FDA Inspection, Mar 6, 2026

Source: https://www.keypedia.com/records/fda_inspections/perma-pure-llc/c7b1b42c-28de-49d3-b73c-1a3714a1e061
Source feed: FDA_Inspections

> FDA inspection 1309030 of Perma Pure LLC, March 06, 2026. Classification: No Action Indicated (NAI). 6 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1309030
- Company Name: Perma Pure LLC
- Inspection Date: 2026-03-06
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Citation Count: 0

## Related Documents

- FDA Inspection 1115239 - 2020-01-03
- [FDA Inspection 956470 - 2016-01-21](https://www.keypedia.com/records/fda_inspections/perma-pure-llc/1f1feebf-bc7a-4e1f-95cd-7136b9f5bb4a)
- FDA Inspection 838041 - 2013-07-09
- [FDA Inspection 745531 - 2011-09-19](https://www.keypedia.com/records/fda_inspections/perma-pure-llc/e70123dc-27fd-49ec-9873-028ac8913f5f)
- [FDA Inspection 713530 - 2011-03-18](https://www.keypedia.com/records/fda_inspections/perma-pure-llc/9adcb502-564e-4e1e-a1c4-3c3887778439)

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/shirley-s-wen/eafbc8e5-a0ac-443a-adaf-ced505f77842)

Company: https://www.keypedia.com/companies/perma-pure-llc/73139477-c364-4c3c-a881-0f88d8a57088