# FDA Inspection 826076 - Interson Corp - March 29, 2013

Source: https://www.globalkeysolutions.net/records/fda_inspections/interson-corp/db50087a-260d-4fc8-acab-d2b3a5056c30
Source feed: FDA_Inspections

> FDA Inspection 826076 for Interson Corp on March 29, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 826076
- Company Name: Interson Corp
- Inspection Date: 2013-03-29
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 826076 - 2013-03-29](https://www.globalkeysolutions.net/records/fda_inspections/interson-corp/2dfadff6-800f-42e9-9919-18284e634c56)
- [FDA Inspection 764313 - 2012-01-20](https://www.globalkeysolutions.net/records/fda_inspections/interson-corp/d7a1857f-fa7a-4f50-bb75-08d52829c4c7)
- [FDA Inspection 764313 - 2012-01-20](https://www.globalkeysolutions.net/records/fda_inspections/interson-corp/7c1fec00-b812-41b3-b9f1-af261b9d96d8)
- [FDA Inspection 647601 - 2010-02-10](https://www.globalkeysolutions.net/records/fda_inspections/interson-corp/4ce734b6-0b42-4f72-bbff-0ea42f989951)
- [FDA Inspection 647601 - 2010-02-10](https://www.globalkeysolutions.net/records/fda_inspections/interson-corp/b673e4bf-f166-42ee-b70f-0c5c543cbef3)

Company: https://www.globalkeysolutions.net/companies/interson-corp/02ac7fb8-7722-4e7e-b1d0-5b913a924caa

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