FDA issued a Warning Letter to Greiner Bio-One North America, Inc. on 4/16/2020 as a result of this inspection.
FDA investigators audited the Greiner Bio-One North America - Monroe, NC, United States facility and issued inspectional observations (via FDA 483) on 13 Dec 2019.
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- Category: Medical Devices & Rad Health
- Inspection end: 13 Dec 2019
- Location: Monroe, United States
- FEI: 3001451379