# FDA Inspection 545232 - Sectra Mamea AB - October 09, 2008

Source: https://www.keypedia.com/records/fda_inspections/sectra-mamea-ab/e9324c1b-e842-453b-94cc-22df1e487ea6
Source feed: FDA_Inspections

> FDA Inspection 545232 for Sectra Mamea AB on October 09, 2008. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 545232
- Company Name: Sectra Mamea AB
- Inspection Date: 2008-10-09
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 545232 - 2008-10-09](https://www.keypedia.com/records/fda_inspections/sectra-mamea-ab/bda3b326-ed32-4b98-bd7c-54f231974207)

Company: https://www.keypedia.com/companies/sectra-mamea-ab/3ba8e0df-734e-4faf-bdcb-f8d4639f785c

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