FDA Inspection 1234386 — ILMO PRODUCTS COMPANY
The FDA completed an inspection of ILMO PRODUCTS COMPANY on Mar 28, 2024 in Jacksonville, IL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Mar 28, 2024
- Fiscal Year
- 2024
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Jacksonville, IL (United States)