FDA Inspection 1028654 — ILMO Products

ILMO Products — FEI 3010164797

The FDA completed an inspection of ILMO Products on Oct 3, 2017 in Granite City, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Oct 3, 2017
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Granite City, IL (United States)