# FDA Inspection 1199112 - Barrett Technology, LLC - March 07, 2023

Source: https://www.keypedia.com/records/fda_inspections/barrett-technology-llc/4843ca1e-14be-4599-aa53-d81f4d4facbf
Source feed: FDA_Inspections

> FDA Inspection 1199112 for Barrett Technology, LLC on March 07, 2023. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1199112
- Company Name: Barrett Technology, LLC
- Inspection Date: 2023-03-07
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1199112 - 2023-03-07](https://www.keypedia.com/records/fda_inspections/barrett-technology-llc/2be24c54-5047-4759-9519-026dedd26f29)
- [FDA Inspection 1036463 - 2017-12-07](https://www.keypedia.com/records/fda_inspections/barrett-technology-llc/c380e726-b7b3-44d6-bed9-bf05aafa2d35)

Company: https://www.keypedia.com/companies/barrett-technology-llc/5450d851-e739-4a54-8221-ab88c7ed8fec

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7