FDA issued a Warning Letter to Cellestis Inc on 8/26/2015 as a result of this inspection.
483 Cellestis Mar 2015

483 Cellestis Mar 2015

Donna Besone FDA$119.00 - Available Now

FDA investigators audited the Cellestis - Santa Clarita, CA, United States facility and issued inspectional observations (via FDA 483) on 25 Mar 2015.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 25 Mar 2015
  • Location: Santa Clarita, United States
  • FEI: 3003964343
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