FDA Inspection
Germiphene CorporationGermiphene Corporation – FDA Inspection, Jun 24, 2010
Record Details
This FDA Inspection record concerns Germiphene Corporation, with an inspection on June 24, 2010, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Germiphene Corporation
- Inspection Date
- June 24, 2010
- Product Type
- Devices
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ID · 3ef7fcc0-2aa3-4bd4-ba5b-ffb84ea89a95
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 671773
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.120(d)Mixups
- 21 CFR 820.100(a)(3)Identification of actions needed
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Other FDA inspections of Germiphene Corporation
3| Date | Classification | Office | Project area |
|---|---|---|---|
| May 24, 2018 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| February 19, 2016 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| March 16, 2012 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Germiphene Corporation
- FDA Inspection 1056647 - 2018-05-24
- FDA Inspection 962166 - 2016-02-19
- FDA Inspection 777994 - 2012-03-16
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