# FDA Inspection 750673 - HemoCue AB - October 26, 2011

Source: https://www.globalkeysolutions.net/records/fda_inspections/hemocue-ab/e8d216e1-2a29-4987-b06b-70ede9f5bbe3
Source feed: FDA_Inspections

> FDA Inspection 750673 for HemoCue AB on October 26, 2011. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 750673
- Company Name: HemoCue AB
- Inspection Date: 2011-10-26
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/hemocue-ab/3e9b45a6-a7c5-4508-aabb-7529e5bb8c0b

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