# FDA Inspection 1018614 - Sanmina Corporation - June 28, 2017

Source: https://www.keypedia.com/records/fda_inspections/sanmina-corporation/9076b99c-7b51-40de-aba6-e63e68b8854b
Source feed: FDA_Inspections

> FDA Inspection 1018614 for Sanmina Corporation on June 28, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1018614
- Company Name: Sanmina Corporation
- Inspection Date: 2017-06-28
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

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- [FDA Inspection 921893 - 2015-04-23](https://www.keypedia.com/records/fda_inspections/sanmina-corporation/76b8298b-2bb1-43ab-8fe9-6539cef00625)
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Company: https://www.keypedia.com/companies/sanmina-corporation/f031a428-0602-4f88-a90c-89ff056cb8f5

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