# FDA Inspection 886118 - Jolife AB - July 02, 2014

Source: https://www.keypedia.com/records/fda_inspections/jolife-ab/5867c079-4df5-49c4-8789-ce7d6bea79ee
Source feed: FDA_Inspections

> FDA Inspection 886118 for Jolife AB on July 02, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 886118
- Company Name: Jolife AB
- Inspection Date: 2014-07-02
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 659849 - 2010-03-24](https://www.keypedia.com/records/fda_inspections/jolife-ab/4b4c1e7d-5f14-4ae7-bbdc-1e1bec26c86b)

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