FDA Documents of Grand River Aseptic Manufacturing, Inc.
Grand River Aseptic Manufacturing, Inc. is an organization that has been audited by the FDA 9 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