# FDA Inspection 1290462 - Nutek Bravo LLC - October 30, 2025

Source: https://www.keypedia.com/records/fda_inspections/nutek-bravo-llc/0b0fd1e4-98e5-40f8-bbf2-6c052d61f1c6
Source feed: FDA_Inspections

> FDA Inspection 1290462 for Nutek Bravo LLC on October 30, 2025. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1290462
- Company Name: Nutek Bravo LLC
- Inspection Date: 2025-10-30
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

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Company: https://www.keypedia.com/companies/nutek-bravo-llc/163ec70a-60c0-47ac-b96c-870771f795c1

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