: Olumide A. Martins
- Olumide A. Martins first started conducting FDA inspections in 2024, with the last inspection in 2024. Over that time, Olumide A. Martins has conducted 3 inspections at 2 companies across 3 sites.
Get Olumide Martins's official FDA inspection documents. Gain valuable insights from their Form 483s and EIRs to ace your next inspection.
Documents
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FDA 483 KBI Biopharma, Inc., Durham | 2024
Out-of-stock
Olumide A. Martins
Human Drugs Form 483
FDA 483 Vetter Pharma Fertigung GmbH & Co. KG (Ravensburg Mooswiesen), Ravensburg | 2024
Out-of-stock
Olumide A. Martins
Human Drugs Form 483