FDA issued a Warning Letter to Cellestis Inc on 8/26/2015 as a result of this inspection.
FDA investigators audited the Cellestis - Santa Clarita, CA, United States facility and issued inspectional observations (via FDA 483) on 25 Mar 2015.
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- Category: Medical Devices & Rad Health
- Inspection end: 25 Mar 2015
- Location: Santa Clarita, United States
- FEI: 3003964343