FDA Inspection 697722 — Genzyme Polyclonals S.A.S.
The FDA completed an inspection of Genzyme Polyclonals S.A.S. on Oct 6, 2010 in Marcy l Etoile. 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: Biologics.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Oct 6, 2010
- Fiscal Year
- 2011
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Marcy l Etoile (France)