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

Source: https://www.keypedia.com/records/fda_inspections/flextronics-america-llc/4edca532-be67-44b9-b3af-d2b8d8798f4d
Source feed: FDA_Inspections

> FDA Inspection 1289810 for Flextronics America LLC on October 30, 2025. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1289810
- Company Name: Flextronics America LLC
- Inspection Date: 2025-10-30
- Classification: Official Action Indicated (OAI)
- Project Area: Compliance: Medical Devices
- Product Type: Medical Devices & Rad Health

## Related Documents

- [FDA Inspection 1289810 - 2025-10-30](https://www.keypedia.com/records/fda_inspections/flextronics-america-llc/c5eb4fdd-9829-4d40-b4d5-213d33f718ac)
- [FDA Inspection 1289810 - 2025-10-30](https://www.keypedia.com/records/fda_inspections/flextronics-america-llc/bb562332-0c33-472b-8f1e-2a7631c3e5b7)
- [FDA Inspection 1289810 - 2025-10-30](https://www.keypedia.com/records/fda_inspections/flextronics-america-llc/7f041243-8a1a-49a3-ab60-642876209c7d)
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Company: https://www.keypedia.com/companies/flextronics-america-llc/3043bb5b-dacc-4385-99e3-08dc498ee4dc
