# Scanfil Atvidaberg AB – FDA Inspection, Sep 27, 2018

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

> FDA inspection 1068594 of Scanfil Atvidaberg AB, September 27, 2018. Classification: No Action Indicated (NAI). 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1068594
- Company Name: Scanfil Atvidaberg AB
- Inspection Date: 2018-09-27
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 886119 - 2014-07-03

## Related Officers

- [Company Rep](https://www.keypedia.com/people/maida-henesian/cd28e878-000c-4af8-8dbd-4863057758bb)

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

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