# Directa AB – FDA Inspection, Sep 5, 2019

Source: https://www.keypedia.com/records/fda_inspections/directa-ab/95369cd0-7081-414b-9d27-2dfb08a6dd04
Source feed: FDA_Inspections

> FDA inspection 1101420 of Directa AB, September 05, 2019. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1101420
- Company Name: Directa AB
- Inspection Date: 2019-09-05
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/matthew-d-schnittker/cf76f07f-db6d-47a0-8412-7eb084d4fe8b)

Company: https://www.keypedia.com/companies/directa-ab/ff1835fd-768d-4c46-af39-c9216435f803

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