FDA Inspection 1083830 — Nusmile, Ltd.

Nusmile, Ltd. — FEI 3006444232

The FDA completed an inspection of Nusmile, Ltd. on Mar 5, 2019 in Houston, TX. 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
Mar 5, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Houston, TX (United States)