# Teka Portugal S.A. – FDA Inspection, Nov 11, 2022

Source: https://www.keypedia.com/records/fda_inspections/teka-portugal-sa/2a3dabe6-6567-45bd-8378-e8e22a173784
Source feed: FDA_Inspections

> FDA inspection 1190353 of Teka Portugal S.A., November 11, 2022. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR parts 1010 and 1030. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1190353
- Company Name: Teka Portugal S.A.
- Inspection Date: 2022-11-11
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- [FDA Inspection 1050401 - 2018-04-27](https://www.keypedia.com/records/fda_inspections/teka-portugal-sa/a3759183-1861-4a42-b46e-548d45556d75)
- [FDA Inspection 970676 - 2016-05-06](https://www.keypedia.com/records/fda_inspections/teka-portugal-sa/2442a5c5-03c4-4d20-8271-8e349181fbe9)

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