FDA Inspection
IBP Medical GmbhIBP Medical Gmbh – FDA Inspection, Nov 12, 2009
Record Details
This FDA Inspection record concerns IBP Medical Gmbh, with an inspection on November 12, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- IBP Medical Gmbh
- Inspection Date
- November 12, 2009
- Product Type
- Devices
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ID · d991bd8e-aaa3-4d94-bff5-42105ef5c68f
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 630049
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
6- 21 CFR 820.80(e)Documentation
- 21 CFR 820.198(a)(3)Processing MDRs {see also 803, 804}
- 21 CFR 820.25(b)Training records
- 21 CFR 820.200(b)Analyzing service report
- 21 CFR 820.50(a)(1)Documented evaluation
- 21 CFR 820.50(b)Supplier notification of changes
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Other FDA inspections of IBP Medical Gmbh
2| Date | Classification | Office | Project area |
|---|---|---|---|
| December 11, 2024 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| May 25, 2018 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for IBP Medical Gmbh
- FDA Inspection 1258331 - 2024-12-11
- FDA Inspection 1053191 - 2018-05-25
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