# FDA Inspection 900361 - Sanmina Ireland Unlimited Company - September 25, 2014

Source: https://www.keypedia.com/records/fda_inspections/sanmina-ireland-unlimited-company/77ad3bed-6447-4b13-9609-86b1d52e4f45
Source feed: FDA_Inspections

> FDA Inspection 900361 for Sanmina Ireland Unlimited Company on September 25, 2014. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 900361
- Company Name: Sanmina Ireland Unlimited Company
- Inspection Date: 2014-09-25
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1217651 - 2023-09-14](https://www.keypedia.com/records/fda_inspections/sanmina-ireland-unlimited-company/4328ebe7-6f83-4d7e-a356-d6893dc99f6b)
- [FDA Inspection 1217651 - 2023-09-14](https://www.keypedia.com/records/fda_inspections/sanmina-ireland-unlimited-company/e5aa10c1-8776-4e46-acd0-fbd491208fb9)

Company: https://www.keypedia.com/companies/sanmina-ireland-unlimited-company/61c6a9ab-8b41-4521-964e-5fdc600a1ad8

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