FDA Inspection 792606 — ILMO PRODUCTS COMPANY

ILMO PRODUCTS COMPANY — FEI 3003574148

The FDA completed an inspection of ILMO PRODUCTS COMPANY on Jul 31, 2012 in Mount Vernon, 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
Jul 31, 2012
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Mount Vernon, IL (United States)