FDA issued a Warning Letter to CellEra LLC on 10/20/2021 as a result of this inspection.
FDA investigators audited the CellEra - Monroe, OH, United States facility and issued inspectional observations (via FDA 483) on 08 Jul 2021.
Product details
- Category: Medical Devices & Rad Health
- Inspection end: 08 Jul 2021
- Location: Monroe, United States
- FEI: 3007594734
