FDA Documents of Grand River Aseptic Manufacturing, Inc.
Grand River Aseptic Manufacturing, Inc. is an organization that has been audited by the FDA 11 times between 2013 and 2024 across all 3 sites.
Documents
FDA 483 Grand River Aseptic Manufacturing | Feb 2024
Available Now - $199
Issued on: Feb 21, 2024
Biologics Form 483
FDA 483 Grand River Aseptic Manufacturing | Jul 2021
Available Now - $199
Issued on: Jul 2, 2021
Human Drug Form 483
FDA EIR Grand River Aseptic Manufacturing | Jun 2018
Available Now - $995
Issued on: Jun 20, 2018
Human Drug Form 483
FDA 483 Grand River Aseptic Manufacturing, Inc., Grand Rapids | 2014
Out-of-stock
Issued on: Nov 24, 2014
Human Drug Form 483
FDA 483 Grand River Aseptic Manufacturing, Inc., Grand Rapids | 2013
Out-of-stock
Issued on: Aug 28, 2013
Biologic Form 483
FDA 483 Grand River Aseptic Manufacturing, Inc., Grand Rapids | 2013
Out-of-stock
Issued on: Feb 22, 2013
Human Drug Form 483
FDA Investigators(14)
- Burnell M. Henry, FDA Investigator
- Alan L. Truong, FDA Investigator
- Susan M. Jackson, FDA Investigator
- Hector A. Carrero, FDA Investigator
- Ou Ma, FDA Investigator
- Joseph A. Piechocki, FDA Investigator
- Charles L. Zhou, FDA Investigator
- Bei Y. He, FDA Investigator
- Lisa R. Hilliard, FDA Investigator
- Constantin Y. Philopoulos, FDA Investigator
- Michele L. Forster, FDA Investigator
- Rebecca E. Dombrowski, FDA Investigator
- Jeffrey D. Meng, FDA Investigator
- Andrew J. Idzior, FDA Investigator