# FDA Inspection 786842 - Flextronics America LLC - June 06, 2012

Source: https://www.keypedia.com/records/fda_inspections/flextronics-america-llc/68283620-3aab-49f0-ac25-44bdeae27432
Source feed: FDA_Inspections

> FDA Inspection 786842 for Flextronics America LLC on June 06, 2012. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 786842
- Company Name: Flextronics America LLC
- Inspection Date: 2012-06-06
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 859108 - 2013-12-27](https://www.keypedia.com/records/fda_inspections/flextronics-america-llc/2bd12e88-4d89-449d-ad2f-b3a9e3309092)

Company: https://www.keypedia.com/companies/flextronics-america-llc/86d51901-b343-434a-9438-a59cf715f283

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