# Germiphene Corporation – FDA Inspection, Jun 24, 2010

Source: https://www.keypedia.com/records/fda_inspections/germiphene-corporation/3ef7fcc0-2aa3-4bd4-ba5b-ffb84ea89a95
Source feed: FDA_Inspections

> FDA inspection 671773 of Germiphene Corporation, June 24, 2010. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 671773
- Company Name: Germiphene Corporation
- Inspection Date: 2010-06-24
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- [FDA Inspection 1056647 - 2018-05-24](https://www.keypedia.com/records/fda_inspections/germiphene-corporation/48d1d854-5177-4987-888d-a1d1c00f267d)
- FDA Inspection 962166 - 2016-02-19
- FDA Inspection 777994 - 2012-03-16

Company: https://www.keypedia.com/companies/germiphene-corporation/0948a001-b5a0-427e-99f4-5dc3f2c36db9

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7