FDA issued a Warning Letter to CellEra LLC on 10/20/2021 for a later inspection.
483 CellEra May 2019

483 CellEra May 2019

Teresa Kastner FDA$119.00 - Available Now

FDA investigators audited the CellEra - Monroe, OH, United States facility and issued inspectional observations (via FDA 483) on 30 May 2019.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 30 May 2019
  • Location: Monroe, United States
  • FEI: 3007594734
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