# FDA Inspection 1068594 - Scanfil Atvidaberg AB - September 27, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/scanfil-atvidaberg-ab/73211628-97d1-4aee-9068-5b5c652f0c0a
Source feed: FDA_Inspections

> FDA Inspection 1068594 for Scanfil Atvidaberg AB on September 27, 2018. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1068594
- Company Name: Scanfil Atvidaberg AB
- Inspection Date: 2018-09-27
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 886119 - 2014-07-03](https://www.globalkeysolutions.net/records/fda_inspections/scanfil-atvidaberg-ab/f1408c13-222a-483b-a916-ce27f0475cda)

Company: https://www.globalkeysolutions.net/companies/scanfil-atvidaberg-ab/452de17e-0190-4b05-a139-fc65de384d34

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