# FDA Inspection 1002325 - Gambro Lundia AB - January 26, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/gambro-lundia-ab/c9e726c8-a990-400b-88d7-dbe6076a24bd
Source feed: FDA_Inspections

> FDA Inspection 1002325 for Gambro Lundia AB on January 26, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1002325
- Company Name: Gambro Lundia AB
- Inspection Date: 2017-01-26
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 907494 - 2014-12-18](https://www.globalkeysolutions.net/records/fda_inspections/gambro-lundia-ab/6c81b59d-40bc-44a4-a34a-fd5e4936886a)
- [FDA Inspection 568201 - 2009-03-05](https://www.globalkeysolutions.net/records/fda_inspections/gambro-lundia-ab/e8ffa388-8787-46b5-bcef-05efb3ebb544)
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Company: https://www.globalkeysolutions.net/companies/gambro-lundia-ab/70e34b05-3fe1-4e15-9bbb-7ec590368d9b

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