FDA Inspection
Meditech KFTMeditech KFT – FDA Inspection, Jan 15, 2015
Record Details
This FDA Inspection record concerns Meditech KFT, with an inspection on January 15, 2015, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Meditech KFT
- Inspection Date
- January 15, 2015
- Product Type
- Devices
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ID · 3b147ba4-038c-4b41-9cd2-71f0cade36ce
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 921149
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.120Lack of or inadequate procedures for labeling
- 21 CFR 820.70(a)Process control procedures, Lack of or inadequate procedures
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Other FDA inspections of Meditech KFT
2| Date | Classification | Office | Project area |
|---|---|---|---|
| June 28, 2018 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| April 13, 2012 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
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