# Dermazone LLC – FDA Inspection, Apr 11, 2019

Source: https://www.keypedia.com/records/fda_inspections/dermazone-llc/676e6519-f0e4-444d-9874-8c50f117ee67
Source feed: FDA_Inspections

> FDA inspection 1086039 of Dermazone LLC, April 11, 2019. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 820. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1086039
- Company Name: Dermazone LLC
- Inspection Date: 2019-04-11
- 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: 4

## Related Documents

- [FDA Inspection 951835 - 2015-11-24](https://www.keypedia.com/records/fda_inspections/dermazone-llc/ae0dfb6b-6863-46df-b29e-a62095ba98c3)
- FDA Inspection 806119 - 2012-11-01
- [FDA Inspection 544410 - 2008-11-05](https://www.keypedia.com/records/fda_inspections/dermazone-llc/13f966de-76a8-4b85-90e3-f48e30439d6d)

## Related Officers

- [Company Rep](https://www.keypedia.com/people/stanley-b-eugene/4708f43e-0592-4c24-b276-d9f9092788a3)

Company: https://www.keypedia.com/companies/dermazone-llc/f871f692-cada-4e9c-bc1f-653b6f849434

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