FDA Investigator: Cheryl J. Legrand
- Cheryl J. Legrand first started conducting FDA inspections in 2000, with the last inspection in 2000. Over that time, Cheryl J. Legrand has conducted 5 inspections at 5 companies across 5 sites.
Get Cheryl Legrand'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 Concordia Clinical Research (IRB), Cedar Knolls | 2000
Out-of-stock
Cheryl J. Legrand
Human Drug Form 483
FDA 483 Garden State Cancer Center, Belleville | 2000
Out-of-stock
Cheryl J. Legrand
Biologic Form 483
FDA 483 St Michael's Medical Center IRB, Newark | 2000
Out-of-stock
Cheryl J. Legrand
Human Drug Form 483