# FDA Inspection 822359 - Cellavision AB - February 28, 2013

Source: https://www.keypedia.com/records/fda_inspections/cellavision-ab/03f8ca9e-5bba-40a6-a538-e39457b9a1a1
Source feed: FDA_Inspections

> FDA Inspection 822359 for Cellavision AB on February 28, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 822359
- Company Name: Cellavision AB
- Inspection Date: 2013-02-28
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 994388 - 2016-11-16](https://www.keypedia.com/records/fda_inspections/cellavision-ab/9968b15f-635c-4196-a543-a890e25ca1bb)

Company: https://www.keypedia.com/companies/cellavision-ab/1bc81891-a120-404a-9dd1-63a6dc1731af

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