# FDA Inspection 669779 - Sanmina Corporation - June 30, 2010

Source: https://www.keypedia.com/records/fda_inspections/sanmina-corporation/0f025f28-e5bb-439f-8230-9d4a3d90f898
Source feed: FDA_Inspections

> FDA Inspection 669779 for Sanmina Corporation on June 30, 2010. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 669779
- Company Name: Sanmina Corporation
- Inspection Date: 2010-06-30
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 996825 - 2016-11-10](https://www.keypedia.com/records/fda_inspections/sanmina-corporation/764772b3-8e73-4f6b-a8c3-55e0e828018c)
- [FDA Inspection 833400 - 2013-05-16](https://www.keypedia.com/records/fda_inspections/sanmina-corporation/e8b97251-e958-4ca4-8d87-3086030dcce6)

Company: https://www.keypedia.com/companies/sanmina-corporation/2a83501a-acca-4e2c-94de-c833b308f2b1

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