# FDA Inspection 1050401 - Teka Portugal S.A. - April 27, 2018

Source: https://www.keypedia.com/records/fda_inspections/teka-portugal-sa/a3759183-1861-4a42-b46e-548d45556d75
Source feed: FDA_Inspections

> FDA Inspection 1050401 for Teka Portugal S.A. on April 27, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1050401
- Company Name: Teka Portugal S.A.
- Inspection Date: 2018-04-27
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/teka-portugal-sa/46959058-ffb6-4c83-ad70-2d258a3948c6

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