FDA Inspection 1112461 — Neocis Inc.

Neocis Inc. — FEI 3012787974

The FDA completed an inspection of Neocis Inc. on Dec 11, 2019 in Miami, FL. 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 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

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