FDA issued a Warning Letter to Sanquin Plasma Products on 8/29/2013 as a result of this inspection.
FDA investigators audited the Sanquin Plasma Supply Foundation - Amsterdam, Netherlands facility and issued inspectional observations (via FDA 483) on 04 Jun 2013.
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- Category: Biologics
- Inspection end: 04 Jun 2013
- Location: Amsterdam, Netherlands
- FEI: 3007166802