FDA issued a Warning Letter to Kelyniam Global, Inc. on 10/5/2017 as a result of this inspection.
FDA investigators audited the Kelyniam Global - Collinsville, CT, United States facility and issued inspectional observations (via FDA 483) on 30 May 2017.
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- Category: Medical Devices & Rad Health
- Inspection end: 30 May 2017
- Location: Collinsville, United States
- FEI: 3009424796