FDA Inspection 1086552 — Medibio USA LLC

Medibio USA LLC — FEI 3014393881

The FDA completed an inspection of Medibio USA LLC on April 16, 2019 in Davie, FL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 3 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
April 16, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Davie, FL (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
41921 CFR 820.20(b)Lack of or inadequate organizational structure
63021 CFR 803.17Lack of Written MDR Procedures