# FDA Inspection 1101420 - Directa AB - September 05, 2019

Source: https://www.keypedia.com/records/fda_inspections/directa-ab/4767c2b3-5282-46f6-a593-6d96727d669c
Source feed: FDA_Inspections

> FDA Inspection 1101420 for Directa AB on September 05, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1101420
- Company Name: Directa AB
- Inspection Date: 2019-09-05
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1101420 - 2019-09-05](https://www.keypedia.com/records/fda_inspections/directa-ab/95369cd0-7081-414b-9d27-2dfb08a6dd04)

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