# FDA Inspection 1309030 - Perma Pure LLC - March 06, 2026

Source: https://www.globalkeysolutions.net/records/fda_inspections/perma-pure-llc/be6fb5d0-e4fb-4e9f-a0b4-d4f367389250
Source feed: FDA_Inspections

> FDA Inspection 1309030 for Perma Pure LLC on March 06, 2026. Classification: No Action Indicated (NAI).

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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)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices

## Related Documents

- [FDA Inspection 1309030 - 2026-03-06](https://www.globalkeysolutions.net/records/fda_inspections/perma-pure-llc/c7b1b42c-28de-49d3-b73c-1a3714a1e061)
- [FDA Inspection 1309030 - 2026-03-06](https://www.globalkeysolutions.net/records/fda_inspections/perma-pure-llc/3bc2051a-bc50-4484-9bc0-901a0bd1d399)
- [FDA Inspection 1115239 - 2020-01-03](https://www.globalkeysolutions.net/records/fda_inspections/perma-pure-llc/2d2d31e9-7eba-4407-bbd5-648c8505665d)
- [FDA Inspection 1115239 - 2020-01-03](https://www.globalkeysolutions.net/records/fda_inspections/perma-pure-llc/9f3c6d65-0429-4174-8072-c6a003754dc1)
- [FDA Inspection 956470 - 2016-01-21](https://www.globalkeysolutions.net/records/fda_inspections/perma-pure-llc/1f1feebf-bc7a-4e1f-95cd-7136b9f5bb4a)

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