# FDA Inspection 1276533 - ATZ Manufacturing - July 24, 2025

Source: https://www.globalkeysolutions.net/records/fda_inspections/atz-manufacturing/2a8720d0-b65f-44cf-a416-6449b3993492
Source feed: FDA_Inspections

> FDA Inspection 1276533 for ATZ Manufacturing on July 24, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1276533
- Company Name: ATZ Manufacturing
- Inspection Date: 2025-07-24
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Office Name: Minneapolis District Office

## Related Documents

- [FDA Inspection 1276533 - 2025-07-24](https://www.globalkeysolutions.net/records/fda_inspections/atz-manufacturing/6832d57d-3811-4313-9a5d-5115be5fabc7)
- [FDA Inspection 1276533 - 2025-07-24](https://www.globalkeysolutions.net/records/fda_inspections/atz-manufacturing/924a2d16-4947-4912-b19d-0883bbc243b6)
- [FDA Inspection 1276533 - 2025-07-24](https://www.globalkeysolutions.net/records/fda_inspections/atz-manufacturing/4e7f1f6a-a7ac-480e-9cfe-60de665e8642)

Company: https://www.globalkeysolutions.net/companies/atz-manufacturing/c199711c-1a04-41bd-9d5e-cfbc9ebfa731

Office: https://www.globalkeysolutions.net/offices/minneapolis-district-office/c79fc8dc-f884-48fc-ba80-2947f662511d