FDA Inspection 1121623 — Reactimex S.A. De C.V.
The FDA completed an inspection of Reactimex S.A. De C.V. on Mar 5, 2020 in Monterrey. 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 5, 2020
- Fiscal Year
- 2020
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Monterrey (Mexico)