FDA Inspection
Teka Portugal S.A.Teka Portugal S.A. – FDA Inspection, May 6, 2016
Record Details
This FDA Inspection record concerns Teka Portugal S.A., with an inspection on May 6, 2016, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Teka Portugal S.A.
- Inspection Date
- May 6, 2016
- Product Type
- Devices
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ID · 2442a5c5-03c4-4d20-8271-8e349181fbe9
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 970676
- FDA center
- Medical Devices & Rad Health
- Project area
- Radiation Control and Health Safety Act
FDA Citations
2- 21 CFR 1030.10(c)(3)(iii)Measurements with tap water container
- 21 CFR 1030.10(c)(3)(i)tests--errors and uncertainties accounted for
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Other FDA inspections of Teka Portugal S.A.
2| Date | Classification | Office | Project area |
|---|---|---|---|
| November 11, 2022 | VAI | Center for Devices and Radiological Health | Radiation Control and Health Safety Act |
| April 27, 2018 | VAI | Center for Devices and Radiological Health | Radiation Control and Health Safety Act |
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