# Universal Pure LLC - Inspection Records

Source: https://www.keypedia.com/companies/universal-pure-llc/137427e2-2987-4719-be16-42d870d32740

> Inspection records and compliance data for Universal Pure LLC in Meriden, Connecticut. Access full analysis and detailed observations.

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## Details

- Name: Universal Pure LLC
- FEI Number: 3009841929
- City: Meriden
- State: Connecticut
- Country Name: United States
- Address Line 1: 65 Chamberlain Hwy
- Zip Code: 06451

## Related Documents

- [FDA Inspection 1283619 - Universal Pure LLC - 2025-12-18](https://www.keypedia.com/records/fda_inspections/universal-pure-llc/e316c873-c576-466a-a90d-46ce5912b757) — source: FDA, date: December 18, 2025
- [FDA Inspection 1125753 - Universal Pure LLC - 2020-07-21](https://www.keypedia.com/records/fda_inspections/universal-pure-llc/5d536d92-61bc-4269-bf5b-35013f5cb959) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 21, 2020
- [FDA Inspection 1099858 - Universal Pure LLC - 2019-08-14](https://www.keypedia.com/records/fda_inspections/universal-pure-llc/2691c25d-e093-48b0-bfee-658f0ed4ffdd) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 14, 2019
- [FDA Inspection 1020183 - Universal Pure LLC - 2017-08-03](https://www.keypedia.com/records/fda_inspections/universal-pure-llc/6b3d6ab6-96d8-49a9-9ddb-93f43dec61b4) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 3, 2017
- [FDA Inspection 981490 - Universal Pure LLC - 2016-08-12](https://www.keypedia.com/records/fda_inspections/universal-pure-llc/a175d7ae-88d4-4938-9186-535f04e75c24) — classification: Official Action Indicated (OAI), source: FDA, date: August 12, 2016
- [FDA Inspection 837130 - Universal Pure LLC - 2013-06-20](https://www.keypedia.com/records/fda_inspections/universal-pure-llc/5f67f41c-6e0f-4db1-ace7-1e0165902384) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 20, 2013
- [FDA Inspection 837130 - Universal Pure LLC - 2013-06-20](https://www.keypedia.com/records/fda_inspections/universal-pure-llc/5de8fade-83e8-436e-bcbf-f0393e107cf1) — classification: No Action Indicated (NAI), source: FDA, date: June 20, 2013

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