# Bioskin LLC – FDA Inspection, Feb 28, 2018

Source: https://www.keypedia.com/records/fda_inspections/bioskin-llc/67f03fb6-b581-4dc0-8998-08a2db07a158
Source feed: FDA_Inspections

> FDA inspection 1042634 of Bioskin LLC, February 28, 2018. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR parts 803 and 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1042634
- Company Name: Bioskin LLC
- Inspection Date: 2018-02-28
- 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: 2

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/james-d-hildreth/1fb2f65a-9905-4848-83a3-16cb1f9e2179)

Company: https://www.keypedia.com/companies/bioskin-llc/7f4b9aca-0c70-4c72-9612-0e54d6c28569

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