FDA Inspection
Medartis AGMedartis AG – FDA Inspection, Aug 27, 2009
Record Details
This FDA Inspection record concerns Medartis AG, with an inspection on August 27, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Medartis AG
- Inspection Date
- August 27, 2009
- Product Type
- Devices
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ID · a2ff6894-582c-4e95-918d-ab0f15b41dcb
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 623342
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.198(a)(1)Uniform and timely processing
- 21 CFR 820.90(a)Nonconforming product notification of responsible parties
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Other FDA inspections of Medartis AG
2| Date | Classification | Office | Project area |
|---|---|---|---|
| July 15, 2024 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| July 30, 2015 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Medartis AG
- FDA Inspection 1246455 - 2024-07-15
- FDA Inspection 940243 - 2015-07-30
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