FDA Documents of Mid America Clinical Laboratories
Mid America Clinical Laboratories is an organization that has been audited by the FDA 11 times between 2001 and 2018 across all 1 sites.
Documents
FDA 483 Mid America Clinical Laboratories, Indianapolis | 2018
Out-of-stock
Issued on: Jun 6, 2018
Biologic Form 483
FDA 483 Mid America Clinical Laboratories, Indianapolis | 2016
Out-of-stock
Issued on: Aug 10, 2016
Biologic Form 483
FDA 483 Mid America Clinical Laboratories, Indianapolis | 2012
Out-of-stock
Issued on: Jun 20, 2012
Biologic Form 483
FDA 483 Mid America Clinical Laboratories, Indianapolis | 2008
Out-of-stock
Issued on: Jun 24, 2008
Biologic Form 483
FDA 483 Mid America Clinical Laboratories, Indianapolis | 2006
Out-of-stock
Issued on: Jul 28, 2006
Biologic Form 483
FDA 483 Mid America Clinical Laboratories, Indianapolis | 2006
Out-of-stock
Issued on: Jun 29, 2006
Biologic Form 483
FDA 483 Mid America Clinical Laboratories, Indianapolis | 2001
Out-of-stock
Issued on: Feb 5, 2001
Biologic Form 483
FDA Investigators(9)
- Travis S. Bradley, FDA Investigator
- Brittany M. Lowe, FDA Investigator
- Matthew J. Gretkierewicz, FDA Investigator
- Dawn C. Olenjack, FDA Investigator
- Nancy L. Neiger, FDA Investigator
- Charles M. Spyr, FDA Investigator
- Helen B. Ricalde, FDA Investigator
- Leigh A. Myers, FDA Investigator
- Lisa P. Oakes, FDA Investigator