# Acuderm, Inc. – FDA Inspection, Jul 13, 2017

Source: https://www.keypedia.com/records/fda_inspections/acuderm-inc/b8ae7ad1-3de0-4869-91dd-36d573b6b2fa
Source feed: FDA_Inspections

> FDA inspection 1017933 of Acuderm, Inc., July 13, 2017. Classification: Voluntary Action Indicated (VAI). 5 citations under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1017933
- Company Name: Acuderm, Inc.
- Inspection Date: 2017-07-13
- 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: 5

## Related Documents

- [FDA Inspection 878759 - 2014-05-09](https://www.keypedia.com/records/fda_inspections/acuderm-inc/fc45bf3e-8f2e-4760-89f4-6e6307c32c6f)
- [FDA Inspection 646620 - 2010-02-19](https://www.keypedia.com/records/fda_inspections/acuderm-inc/d956a69c-b20d-4c68-90ae-45bb2e9ed9d2)

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/karen-m-cruz-arenas/6c698301-84ca-4ba7-a79c-309721db2f1b)

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