# Gambro Lundia AB – FDA Inspection, Jan 26, 2017

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

> FDA inspection 1002325 of Gambro Lundia AB, January 26, 2017. Classification: No Action Indicated (NAI). 2 other FDA inspections on record for this company.

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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)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 907494 - 2014-12-18
- FDA Inspection 568201 - 2009-03-05

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/james-r-montero/ce2d19fd-25b7-423e-9132-5d6f582380d2)

Company: https://www.keypedia.com/companies/gambro-lundia-ab/70e34b05-3fe1-4e15-9bbb-7ec590368d9b

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