FDA issued a Warning Letter to Greiner Bio-One North America, Inc. on 4/16/2020 as a result of this inspection.
483 Greiner Bio-One North America Dec 2019

483 Greiner Bio-One North America Dec 2019

Matthew Humbard FDA, Edward Lockwood FDA, David Lowe FDA$119.00 - Available Now

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.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 13 Dec 2019
  • Location: Monroe, United States
  • FEI: 3001451379
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