FDA issued a Warning Letter to CORPAK MedSystems, Inc. on 4/10/2013 as a result of this inspection.
483 CORPAK MedSystems Jan 2013
483 CORPAK MedSystems Jan 2013Andrew Leboeuf FDA$119.00 - Available Now
FDA investigators audited the CORPAK MedSystems - Buffalo Grove, IL, United States facility and issued inspectional observations (via FDA 483) on 04 Jan 2013.
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- Category: Medical Devices & Rad Health
- Inspection end: 04 Jan 2013
- Location: Buffalo Grove, United States
- FEI: 1419949