FDA issued a Warning Letter to Cordis LLC on 2/16/2011 as a result of this inspection.
FDA investigators audited the Cordis - San German, PR, United States facility and issued inspectional observations (via FDA 483) on 13 Oct 2010.
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- Category: Medical Devices & Rad Health
- Inspection end: 13 Oct 2010
- Location: San German, United States
- FEI: 3003742446