# FDA Inspection 803780 - Fredriksons Verkstad AB - October 12, 2012

Source: https://www.keypedia.com/records/fda_inspections/fredriksons-verkstad-ab/e5a7ceef-ffb9-4cdb-adb0-7f11b5bb1f0e
Source feed: FDA_Inspections

> FDA Inspection 803780 for Fredriksons Verkstad AB on October 12, 2012. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 803780
- Company Name: Fredriksons Verkstad AB
- Inspection Date: 2012-10-12
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 803780 - 2012-10-12](https://www.keypedia.com/records/fda_inspections/fredriksons-verkstad-ab/d8db58d0-afb8-4bdf-a737-0b5549078d59)

Company: https://www.keypedia.com/companies/fredriksons-verkstad-ab/59548e2a-92f7-4993-8a42-8c17016d65b6

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