# Lumazu LLC - Inspection Records

Source: https://www.keypedia.com/companies/lumazu-llc/25bbedee-7f7f-46bf-880c-c09f25a660c9

> Inspection records and compliance data for Lumazu LLC in Lake Luzerne, New York. Access full analysis and detailed observations.

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## Details

- Name: Lumazu LLC
- FEI Number: 3004026600
- City: Lake Luzerne
- State: New York
- Country Name: United States
- Address Line 1: 1256 Lake Ave
- Zip Code: 12846

## Related Documents

- [FDA Inspection 1228207 - Lumazu LLC - 2024-01-22](https://www.keypedia.com/records/fda_inspections/lumazu-llc/caa28ec2-0b6c-48ed-9ba0-d435d0ed4d69) — classification: No Action Indicated (NAI), source: FDA, date: January 22, 2024
- [FDA Inspection 1228207 - Lumazu LLC - 2024-01-22](https://www.keypedia.com/records/fda_inspections/lumazu-llc/d71d4957-94af-48ef-b2c9-93be77eb04df) — classification: No Action Indicated (NAI), source: FDA, date: January 22, 2024
- [FDA Inspection 1142516 - Lumazu LLC - 2021-05-11](https://www.keypedia.com/records/fda_inspections/lumazu-llc/0b326b26-54df-474c-a9fb-fb328fa07e1e) — classification: No Action Indicated (NAI), source: FDA, date: May 11, 2021
- [FDA Inspection 1038606 - Lumazu LLC - 2018-01-25](https://www.keypedia.com/records/fda_inspections/lumazu-llc/6a80d47e-c8ef-4d73-9065-06400e81259e) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 25, 2018
- [FDA Inspection 911198 - Lumazu LLC - 2015-01-21](https://www.keypedia.com/records/fda_inspections/lumazu-llc/fbc2dd59-de82-45f0-ab78-a95c33a8b018) — classification: No Action Indicated (NAI), source: FDA, date: January 21, 2015
- [FDA Inspection 803102 - Lumazu LLC - 2012-10-15](https://www.keypedia.com/records/fda_inspections/lumazu-llc/d2872354-b489-435a-940c-53d674c33a7b) — classification: No Action Indicated (NAI), source: FDA, date: October 15, 2012
- [FDA Inspection 803102 - Lumazu LLC - 2012-10-15](https://www.keypedia.com/records/fda_inspections/lumazu-llc/b8605347-0367-44a3-968f-b3f59490d12e) — classification: No Action Indicated (NAI), source: FDA, date: October 15, 2012

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