FDA Inspection 1112461 — Neocis Inc.

Neocis Inc. — FEI 3012787974

The FDA completed an inspection of Neocis Inc. on December 11, 2019 in Miami, FL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
December 11, 2019
Fiscal Year
2020
Product Type
Devices
Project Area
Compliance: Devices
Location
Miami, FL (United States)

Citations

IDCFRDescription
48621 CFR 820.50(a)Evaluation of suppliers, contractors, etc., requirements