FDA Documents of Sciarra Laboratories, Inc.
Sciarra Laboratories, Inc. is an organization that has been audited by the FDA 19 times between 2000 and 2023 across all 2 sites.
Documents
FDA 483 Sciarra Laboratories, Hicksville | August 2023
Available Now - $199
Issued on: Aug 7, 2023
Human Drugs Form 483
FDA 483 Sciarra Laboratories, Inc., Hicksville | 2018
Out-of-stock
Issued on: Mar 29, 2018
Medical Devices & Rad Health Form 483
FDA 483 Sciarra Laboratories, Inc., Hicksville | 2011
Out-of-stock
Issued on: Jun 3, 2011
Human Drug Form 483
FDA 483 Sciarra Laboratories, Inc., Hicksville | 2007
Out-of-stock
Issued on: Sep 6, 2007
Human Drug Form 483
FDA 483 Sciarra Laboratories, Inc., Hicksville | 2001
Out-of-stock
Issued on: Oct 31, 2001
Human Drug Form 483
FDA 483 Sciarra Laboratories, Inc., Hicksville | 2000
Out-of-stock
Issued on: Oct 5, 2000
Human Drug Form 483
FDA 483 Sciarra Laboratories, Inc., Hicksville | 2000
Out-of-stock
Issued on: Apr 17, 2000
Human Drug Form 483
FDA Investigators(14)
- Gam S. Zamil, FDA Investigator
- Karishma G. Gopaul, FDA Investigator
- Jacqueline S. Warner, FDA Investigator
- Robert C. Horan, FDA Investigator
- Demitria J. Xiradakis, FDA Investigator
- Charisse K. Green, FDA Investigator
- James A. Liubicich, FDA Investigator
- Robert C. Steyert, FDA Investigator
- Ronald Ifraimov, FDA Investigator
- Uduak M. Inokon, FDA Investigator
- Alice S. Tsao, FDA Investigator
- Thomas J. Mooney, FDA Investigator
- Paul C. Mouris, FDA Investigator
- Peter Abel, FDA Investigator