# PRO-TECH Design & Mfg., Inc. - Inspection Records

Source: https://www.keypedia.com/companies/pro-tech-design-mfg-inc/f84ae588-49bd-4504-af30-a1818fd1927e

> Inspection records and compliance data for PRO-TECH Design & Mfg., Inc. in Arlington, Texas. Access full analysis and detailed observations.

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## Details

- Name: PRO-TECH Design & Mfg., Inc.
- FEI Number: 3010531069
- City: Arlington
- State: Texas
- Country Name: United States
- Address Line 1: 4041 Express St
- Zip Code: 76001

## Related Documents

- [483 - PRO-TECH Design & Mfg., Inc. - 2025-04-14](https://www.keypedia.com/records/483/pro-tech-design-mfg-inc/623ff002-4125-4ae1-b2af-cc9a05d95b7d) — source: FDA, date: April 14, 2025
- [FDA Inspection 1266828 - PRO-TECH Design & Mfg., Inc. - 2025-04-14](https://www.keypedia.com/records/fda_inspections/pro-tech-design-mfg-inc/d6f80aac-ec9b-4bd8-be6a-de336629c35a) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 14, 2025
- [FDA Inspection 1266828 - PRO-TECH Design & Mfg., Inc. - 2025-04-14](https://www.keypedia.com/records/fda_inspections/pro-tech-design-mfg-inc/3c142664-56b2-4ae3-99ec-2a14d5d121b8) — classification: No Action Indicated (NAI), source: FDA, date: April 14, 2025
- [FDA Inspection 1266828 - PRO-TECH Design & Mfg., Inc. - 2025-04-14](https://www.keypedia.com/records/fda_inspections/pro-tech-design-mfg-inc/e0695611-6995-45a4-89bf-d282bc81e00e) — classification: No Action Indicated (NAI), source: FDA, date: April 14, 2025
- [FDA Inspection 1266828 - PRO-TECH Design & Mfg., Inc. - 2025-04-14](https://www.keypedia.com/records/fda_inspections/pro-tech-design-mfg-inc/b30dcc10-bbd0-464d-88a2-0224eac2b0e4) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 14, 2025
- [FDA Inspection 1167111 - PRO-TECH Design & Mfg., Inc. - 2022-03-28](https://www.keypedia.com/records/fda_inspections/pro-tech-design-mfg-inc/8e82ad3a-05f4-41c3-bbd4-bf843eebc2d9) — classification: No Action Indicated (NAI), source: FDA, date: March 28, 2022
- [FDA Inspection 1167111 - PRO-TECH Design & Mfg., Inc. - 2022-03-28](https://www.keypedia.com/records/fda_inspections/pro-tech-design-mfg-inc/afe65c8c-a9b5-4478-a58c-d9ed4cbe7845) — classification: No Action Indicated (NAI), source: FDA, date: March 28, 2022
- [FDA Inspection 1041793 - PRO-TECH Design & Mfg., Inc. - 2018-01-25](https://www.keypedia.com/records/fda_inspections/pro-tech-design-mfg-inc/7b6f685c-46c0-4498-a44d-edd21112c6dc) — classification: No Action Indicated (NAI), source: FDA, date: January 25, 2018
- [FDA Inspection 1041793 - PRO-TECH Design & Mfg., Inc. - 2018-01-25](https://www.keypedia.com/records/fda_inspections/pro-tech-design-mfg-inc/3424c0c9-3adf-42ad-a899-1a79f2d792f4) — classification: No Action Indicated (NAI), source: FDA, date: January 25, 2018
- [FDA Inspection 960833 - PRO-TECH Design & Mfg., Inc. - 2016-02-29](https://www.keypedia.com/records/fda_inspections/pro-tech-design-mfg-inc/0b9af3bd-6ead-4a1d-a237-8d8b89d77c4a) — classification: No Action Indicated (NAI), source: FDA, date: February 29, 2016
- [FDA Inspection 960833 - PRO-TECH Design & Mfg., Inc. - 2016-02-29](https://www.keypedia.com/records/fda_inspections/pro-tech-design-mfg-inc/9154cbbb-551a-4f93-b0ea-7ee976ba53d2) — classification: No Action Indicated (NAI), source: FDA, date: February 29, 2016

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