# FDA Inspection 652647 - Vitrolife Sweden AB - February 18, 2010

Source: https://www.keypedia.com/records/fda_inspections/vitrolife-sweden-ab/0bc03ae7-3c50-4bfd-9e54-c4152a49cb39
Source feed: FDA_Inspections

> FDA Inspection 652647 for Vitrolife Sweden AB on February 18, 2010. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 652647
- Company Name: Vitrolife Sweden AB
- Inspection Date: 2010-02-18
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/vitrolife-sweden-ab/858a164c-7970-4eec-8db8-8f8b14722939

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