# Teka Portugal S.A. – FDA Inspection, May 6, 2016

Source: https://www.keypedia.com/records/fda_inspections/teka-portugal-sa/2442a5c5-03c4-4d20-8271-8e349181fbe9
Source feed: FDA_Inspections

> FDA inspection 970676 of Teka Portugal S.A., May 06, 2016. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 1030. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 970676
- Company Name: Teka Portugal S.A.
- Inspection Date: 2016-05-06
- 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

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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