FDA Inspection 967729 — Ali A. Valika

Ali A. Valika — FEI 3012136613

The FDA completed an inspection of Ali A. Valika on February 26, 2016 in Elmhurst, IL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
February 26, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Elmhurst, IL (United States)

Additional Details

Clinical Investigator (CI)