FDA Inspection 1040166 — ILMO PRODUCTS COMPANY
The FDA completed an inspection of ILMO PRODUCTS COMPANY on Feb 1, 2018 in Quincy, 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
- Feb 1, 2018
- Fiscal Year
- 2018
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Quincy, IL (United States)