FDA Inspection 1178941 — Incoba LLC

Incoba LLC — FEI 3017865349

The FDA completed an inspection of Incoba LLC on Aug 19, 2022 in Chesterfield, 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). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Aug 19, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Compliance: Devices
Location
Chesterfield, MO (United States)