FDA Inspection 1162079 — Skin Vision BV

Skin Vision BV — FEI 3020462697

The FDA completed an inspection of Skin Vision BV on Jan 21, 2022 in Amsterdam. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jan 21, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Amsterdam (Netherlands)

Additional Details

Sponsor, Contract Research Organization

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.