FDA Inspection 1158153 — Artemis Bio-Solutions
The FDA completed an inspection of Artemis Bio-Solutions on Dec 1, 2021 in Wood Dale, 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
- Dec 1, 2021
- Fiscal Year
- 2022
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Wood Dale, IL (United States)