FDA issued a Warning Letter to Cenorin, LLC on 2/12/2015 as a result of this inspection.
FDA investigators audited the Cenorin - Kent, WA, United States facility and issued 3 inspectional observations (via FDA 483) on 02 May 2014.
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- Category: Medical Devices & Rad Health
- Number of Observations: 3
- Inspection end: 02 May 2014
- Location: Kent, United States
- FEI: 3004153171