FDA Investigator: Miah I. Schneider
- Miah I. Schneider first started conducting FDA inspections in 2000, with the last inspection in 2009. Over that time, Miah I. Schneider has conducted 10 inspections at 10 companies across 10 sites.
Get Miah Schneider'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 JHP Pharmaceuticals, LLC, Rochester | 2009
Out-of-stock
Miah I. Schneider
Human Drug Form 483
FDA 483 Caraco Pharmaceutical Laboratories, LTD., Detroit | 2006
Out-of-stock
Miah I. Schneider
Human Drug Form 483
FDA 483 Genesis Pharmaceutical, Inc., Henderson | 2000
Out-of-stock
Miah I. Schneider
Human Drug Form 483
FDA 483 W.A. Foote Memorial Hospital, Inc-IRC, Jackson | 2000
Out-of-stock
Miah I. Schneider
Biologic Form 483
FDA 483 Biological Research Solutions, Inc., Rochester Hills | 2000
Out-of-stock
Miah I. Schneider
Human Drug Form 483
FDA 483 Elba, Inc. dba Elba Laboratories, Troy | 2000
Out-of-stock
Miah I. Schneider
Human Drug Form 483
FDA 483 Ferndale Laboratories, Inc., Ferndale | 2000
Out-of-stock
Miah I. Schneider
Human Drug Form 483
Co-Investigators (10)
- Rebecca E. Dombrowski, FDA Investigator
- Salwa K. Poole, FDA Investigator
- Azza Talaat, FDA Investigator
- Patsy J. Domingo, FDA Investigator
- Roger A. Hartman, FDA Investigator
- Renee L. Rice, FDA Investigator
- Catherine V. Quinlan, FDA Investigator
- Judith A. Jankowski, FDA Investigator
- Reginald Walker, FDA Investigator
- Leslie A. Paul, FDA Investigator