FDA Investigator: Shari L. Kahn
- Shari L. Kahn first started conducting FDA inspections in 2000, with the last inspection in 2001. Over that time, Shari L. Kahn has conducted 24 inspections at 21 companies across 21 sites.
Get Shari Kahn'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 Bristol-myers Squibb Pharma Company, Garden City | 2001
Out-of-stock
Shari L. Kahn
Human Drug Form 483
FDA 483 Time-Cap Laboratories, Inc., Farmingdale | 2001
Out-of-stock
Shari L. Kahn
Human Drug Form 483
FDA 483 Bristol-myers Squibb Pharma Company, Garden City | 2001
Out-of-stock
Shari L. Kahn
Human Drug Form 483
FDA 483 Endo Pharmaceutical, Inc., Westbury | 2001
Out-of-stock
Shari L. Kahn
Human Drug Form 483
FDA 483 Perrigo New York, Bronx | 2000
Out-of-stock
Shari L. Kahn
Human Drug Form 483
FDA 483 Luitpold Pharmaceuticals, Inc., Shirley | 2000
Out-of-stock
Shari L. Kahn
Biologic Form 483