# HemoCue AB – FDA Inspection, May 31, 2018

Source: https://www.keypedia.com/records/fda_inspections/hemocue-ab/db416814-882f-4940-9399-11a7cf2a31a1
Source feed: FDA_Inspections

> FDA inspection 1055264 of HemoCue AB, May 31, 2018. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1055264
- Company Name: HemoCue AB
- Inspection Date: 2018-05-31
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- FDA Inspection 825448 - 2013-03-20
- FDA Inspection 750673 - 2011-10-26

## Related Officers

- [Company Rep](https://www.keypedia.com/people/john-a-sciacchitano/9f8f49bf-1971-449e-972e-b516418ea78e)

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

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