# Acuderm, Inc. – FDA Inspection, Feb 19, 2010

Source: https://www.keypedia.com/records/fda_inspections/acuderm-inc/d956a69c-b20d-4c68-90ae-45bb2e9ed9d2
Source feed: FDA_Inspections

> FDA inspection 646620 of Acuderm, Inc., February 19, 2010. Classification: Voluntary Action Indicated (VAI). 2 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 646620
- Company Name: Acuderm, Inc.
- Inspection Date: 2010-02-19
- 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: 0

## Related Documents

- [FDA Inspection 1017933 - 2017-07-13](https://www.keypedia.com/records/fda_inspections/acuderm-inc/b8ae7ad1-3de0-4869-91dd-36d573b6b2fa)
- [FDA Inspection 878759 - 2014-05-09](https://www.keypedia.com/records/fda_inspections/acuderm-inc/fc45bf3e-8f2e-4760-89f4-6e6307c32c6f)

Company: https://www.keypedia.com/companies/acuderm-inc/9dd97a4d-a9f0-4ae2-8c49-d9b4765fe034

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