# Acuderm, Inc. – FDA Inspection, May 9, 2014

Source: https://www.keypedia.com/records/fda_inspections/acuderm-inc/fc45bf3e-8f2e-4760-89f4-6e6307c32c6f
Source feed: FDA_Inspections

> FDA inspection 878759 of Acuderm, Inc., May 09, 2014. Classification: Voluntary Action Indicated (VAI). 5 citations under 21 CFR part 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 878759
- Company Name: Acuderm, Inc.
- Inspection Date: 2014-05-09
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 5

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- [FDA Inspection 1017933 - 2017-07-13](https://www.keypedia.com/records/fda_inspections/acuderm-inc/b8ae7ad1-3de0-4869-91dd-36d573b6b2fa)
- [FDA Inspection 646620 - 2010-02-19](https://www.keypedia.com/records/fda_inspections/acuderm-inc/d956a69c-b20d-4c68-90ae-45bb2e9ed9d2)

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