FDA issued a Warning Letter to Covidien LP on 6/14/2012 as a result of this inspection.
FDA investigators audited the Covidien, LP - North Haven, CT, United States facility and issued inspectional observations (via FDA 483) on 09 Feb 2012.
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- Category: Medical Devices & Rad Health
- Inspection end: 09 Feb 2012
- Location: North Haven, United States
- FEI: 1219930