FDA Inspection 1157912 — NANOFIBER SOLUTIONS, INC

NANOFIBER SOLUTIONS, INC — FEI 3014527904

The FDA completed an inspection of NANOFIBER SOLUTIONS, INC on Oct 29, 2021 in Dublin, OH. 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
Oct 29, 2021
Fiscal Year
2022
Product Type
Devices
Project Area
Compliance: Devices
Location
Dublin, OH (United States)

Citations

IDCFRDescription
54621 CFR 820.75(a)Lack of or inadequate process validation

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