# FDA Inspection 1274225 - Pro-Tech Design & Mfg. Inc. - June 27, 2025

Source: https://www.globalkeysolutions.net/records/fda_inspections/pro-tech-design-mfg-inc/10bd31ac-f3d1-409d-9c1a-acbf9a08dacf
Source feed: FDA_Inspections

> FDA Inspection 1274225 for Pro-Tech Design & Mfg. Inc. on June 27, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1274225
- Company Name: Pro-Tech Design & Mfg. Inc.
- Inspection Date: 2025-06-27
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Office Name: Los Angeles District Office

## Related Documents

- [FDA Inspection 1274225 - 2025-06-27](https://www.globalkeysolutions.net/records/fda_inspections/pro-tech-design-mfg-inc/f369aa74-3ce1-4f4c-8ed4-776fe2119f70)
- [FDA Inspection 1165844 - 2022-03-16](https://www.globalkeysolutions.net/records/fda_inspections/pro-tech-design-mfg-inc/d449fada-dc6e-4b4b-8bfa-2ef64af201ea)
- [FDA Inspection 1063762 - 2018-03-16](https://www.globalkeysolutions.net/records/fda_inspections/pro-tech-design-mfg-inc/47b37eb7-df0d-4b3e-a213-6b704684e720)
- [FDA Inspection 989126 - 2016-07-27](https://www.globalkeysolutions.net/records/fda_inspections/pro-tech-design-mfg-inc/6333834d-9d96-4428-889a-7d00d9f6d36e)
- [FDA Inspection 989126 - 2016-07-27](https://www.globalkeysolutions.net/records/fda_inspections/pro-tech-design-mfg-inc/c8ff628e-a7cc-41f6-8132-a3e943d4530f)

Company: https://www.globalkeysolutions.net/companies/pro-tech-design-mfg-inc/48cb121e-511f-4b89-914b-507ccc03ef34

Office: https://www.globalkeysolutions.net/offices/los-angeles-district-office/edcf1dfe-596a-43b8-8df4-07d9cd94763b