# FDA Inspection 1029104 - Newport Corp. - October 04, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/newport-corp/e990f4b1-fdd8-47f2-9370-61719d6f16e9
Source feed: FDA_Inspections

> FDA Inspection 1029104 for Newport Corp. on October 04, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1029104
- Company Name: Newport Corp.
- Inspection Date: 2017-10-04
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1029104 - 2017-10-04](https://www.globalkeysolutions.net/records/fda_inspections/newport-corp/2b3f070c-1d6e-4fa1-89f3-98630b70b34f)
- [FDA Inspection 746972 - 2011-09-23](https://www.globalkeysolutions.net/records/fda_inspections/newport-corp/211ff060-8db4-4fc8-a518-521bfc72d41c)

Company: https://www.globalkeysolutions.net/companies/newport-corp/40880ea1-110e-4b9b-aa5b-d6b91c545c8b

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