# FDA Inspection 659849 - Jolife AB - March 24, 2010

Source: https://www.keypedia.com/records/fda_inspections/jolife-ab/4b4c1e7d-5f14-4ae7-bbdc-1e1bec26c86b
Source feed: FDA_Inspections

> FDA Inspection 659849 for Jolife AB on March 24, 2010. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 659849
- Company Name: Jolife AB
- Inspection Date: 2010-03-24
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 886118 - 2014-07-02](https://www.keypedia.com/records/fda_inspections/jolife-ab/5867c079-4df5-49c4-8789-ce7d6bea79ee)

Company: https://www.keypedia.com/companies/jolife-ab/170cf61c-9dd9-466b-896a-388d06086a79

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