FDA Inspection 1208569 — Aeropres Corporation

Aeropres Corporation — FEI 3027071754

The FDA completed an inspection of Aeropres Corporation on June 22, 2023 in Morris, IL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 22, 2023
Fiscal Year
2023
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Morris, IL (United States)