FDA Investigator: Soyinka S. Eneng
- Soyinka S. Eneng first started conducting FDA inspections in 2022, with the last inspection in 2024. Over that time, Soyinka S. Eneng has conducted 11 inspections at 10 companies across 10 sites.
Get Soyinka Eneng'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 AML Riverside, Fort Dodge | August 2023
Available Now - $199
Soyinka S. Eneng
Animal Drugs & Feeds Form 483
FDA 483 Upsher-Smith Laboratories, LLC, Maple Grove | 2024
Out-of-stock
Soyinka S. Eneng
Human Drugs Form 483
FDA 483 Coloplast Manufacturing US, LLC, North Mankato | 2024
Out-of-stock
Soyinka S. Eneng
Human Drugs Form 483
FDA 483 Ash Stevens LLC, Riverview | 2024
Out-of-stock
Soyinka S. Eneng
Human Drugs Form 483
FDA 483 Lloyd Inc. of Iowa, Shenandoah | 2023
Out-of-stock
Soyinka S. Eneng
Animal Drugs & Feeds Form 483
FDA 483 Upsher-Smith Laboratories, LLC, Maple Grove | 2022
Out-of-stock
Soyinka S. Eneng
Human Drug Form 483
FDA 483 CHRI Laboratories, Inc., Saint Paul | 2022
Out-of-stock
Soyinka S. Eneng
Human Drug Form 483
Co-Investigators (11)
- Rafeeq A. Habeeb, FDA Investigator
- Beatrix D. Hippe,
- Nicholas J. Presto, FDA Investigator
- Matthew B. Casale, FDA Investigator
- Kevin P. Regan, FDA Investigator
- Beatrix D. Arevalo,
- Michele Perry-Williams, FDA Investigator
- Michele L. Glendenning, FDA Investigator
- Krista K. Petersen, FDA Investigator
- Courtney R. Ingalsbe, FDA Investigator
- Ross J. Grigsby, FDA Investigator