FDA Inspection 1034225 — Nanova Biomaterials Inc

Nanova Biomaterials Inc — FEI 3011430871

The FDA completed an inspection of Nanova Biomaterials Inc on Dec 8, 2017 in Columbia, MO. 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). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Dec 8, 2017
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Columbia, MO (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures