# Lutech Industries Inc - Inspection Records

Source: https://www.keypedia.com/companies/lutech-industries-inc/b0b8d4ca-8cb9-4b53-811a-b827525ebdcb

> Inspection records and compliance data for Lutech Industries Inc in Ronkonkoma, New York. Access full analysis and detailed observations.

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## Details

- Name: Lutech Industries Inc
- FEI Number: 3010023733
- City: Ronkonkoma
- State: New York
- Country Name: United States
- Address Line 1: 105 Remington Blvd Ste C
- Zip Code: 11779

## Related Documents

- [483 - Lutech Industries Inc - 2025-03-26](https://www.keypedia.com/records/483/lutech-industries-inc/495a7cb4-ecb1-4204-8c50-4a1519f6028a) — source: FDA, date: March 26, 2025
- [FDA Inspection 1266521 - Lutech Industries Inc - 2025-03-26](https://www.keypedia.com/records/fda_inspections/lutech-industries-inc/84c13dad-2dd9-492f-afc1-92c236516d5d) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 26, 2025
- [FDA Inspection 1266521 - Lutech Industries Inc - 2025-03-26](https://www.keypedia.com/records/fda_inspections/lutech-industries-inc/17f59718-6dc9-42f0-83eb-ba2ce38b9319) — classification: No Action Indicated (NAI), source: FDA, date: March 26, 2025
- [FDA Inspection 1266521 - Lutech Industries Inc - 2025-03-26](https://www.keypedia.com/records/fda_inspections/lutech-industries-inc/b33b342a-89a9-450f-a9f8-50cb5809c486) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 26, 2025
- [FDA Inspection 1266521 - Lutech Industries Inc - 2025-03-26](https://www.keypedia.com/records/fda_inspections/lutech-industries-inc/aa6900f7-25e7-4a1f-bfb5-ef5eee669fdd) — classification: No Action Indicated (NAI), source: FDA, date: March 26, 2025
- [FDA Inspection 1154488 - Lutech Industries Inc - 2021-09-10](https://www.keypedia.com/records/fda_inspections/lutech-industries-inc/a7f81c7f-1f01-4733-92bc-ce14cf289857) — classification: No Action Indicated (NAI), source: FDA, date: September 10, 2021
- [FDA Inspection 1154488 - Lutech Industries Inc - 2021-09-10](https://www.keypedia.com/records/fda_inspections/lutech-industries-inc/7065c5ec-fef0-45f0-ad9b-7a37b64d3afb) — classification: No Action Indicated (NAI), source: FDA, date: September 10, 2021
- [FDA Inspection 1028481 - Lutech Industries Inc - 2017-10-12](https://www.keypedia.com/records/fda_inspections/lutech-industries-inc/012986ce-063f-40ac-8c26-afa6576dc76c) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 12, 2017
- [FDA Inspection 941321 - Lutech Industries Inc - 2015-07-17](https://www.keypedia.com/records/fda_inspections/lutech-industries-inc/27f7818a-3b46-4e46-a955-183c712e4046) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 17, 2015
- [FDA Inspection 852478 - Lutech Industries Inc - 2013-10-18](https://www.keypedia.com/records/fda_inspections/lutech-industries-inc/0c22f680-a304-48dc-a1d5-9349abc1a6b4) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 18, 2013
- [FDA Inspection 852478 - Lutech Industries Inc - 2013-10-18](https://www.keypedia.com/records/fda_inspections/lutech-industries-inc/3cc1fee0-06fa-4065-8d79-b3f0ed8edb3d) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 18, 2013

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