# FDA Inspection 1289810 - Flextronics America LLC - October 30, 2025

Source: https://www.keypedia.com/records/fda_inspections/flextronics-america-llc/c5eb4fdd-9829-4d40-b4d5-213d33f718ac
Source feed: FDA_Inspections

> FDA Inspection 1289810 for Flextronics America LLC on October 30, 2025. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1289810
- Company Name: Flextronics America LLC
- Inspection Date: 2025-10-30
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Office Name: Dallas District Office

## Related Documents

- [FDA Inspection 1289810 - 2025-10-30](https://www.keypedia.com/records/fda_inspections/flextronics-america-llc/4edca532-be67-44b9-b3af-d2b8d8798f4d)
- [FDA Inspection 1289810 - 2025-10-30](https://www.keypedia.com/records/fda_inspections/flextronics-america-llc/bb562332-0c33-472b-8f1e-2a7631c3e5b7)
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Company: https://www.keypedia.com/companies/flextronics-america-llc/3043bb5b-dacc-4385-99e3-08dc498ee4dc

Office: https://www.keypedia.com/offices/dallas-district-office/2d1ee9ae-c44c-4494-8186-a920a69b98f9