FDA Inspection
Medi-Globe GmbHMedi-Globe GmbH – FDA Inspection, Oct 20, 2010
Record Details
This FDA Inspection record concerns Medi-Globe GmbH, with an inspection on October 20, 2010, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Medi-Globe GmbH
- Inspection Date
- October 20, 2010
- Product Type
- Devices
View Company Profile
ID · a174cab2-6071-4664-aed6-a89916860e0a
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 698625
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
FDA Citations
3- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
- 21 CFR 803.17(a)(1)Lack of System for Event Evaluations
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Other FDA inspections of Medi-Globe GmbH
1| Date | Classification | Office | Project area |
|---|---|---|---|
| February 18, 2015 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Medi-Globe GmbH
- FDA Inspection 917419 - 2015-02-18
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