FDA Inspection 635392 — OMRIX Biopharmaceuticals Ltd.
The FDA completed an inspection of OMRIX Biopharmaceuticals Ltd. on Oct 29, 2009 in Ramat Gan. 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 29, 2009
- Fiscal Year
- 2010
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Ramat Gan (Israel)