FDA Documents of Rechon Life Science AB
Rechon Life Science AB is an organization that has been audited by the FDA 10 times between 2001 and 2023 across all 1 sites.
Documents
FDA 483 Rechon Life Science AB, Limhamn | 2023
Out-of-stock
Issued on: Mar 17, 2023
Human Drugs Form 483
FDA 483 Rechon Life Science AB, Limhamn | 2018
Out-of-stock
Issued on: Jun 29, 2018
Human Drug Form 483
FDA 483 Rechon Life Science AB, Limhamn | 2016
Out-of-stock
Issued on: Apr 29, 2016
Human Drug Form 483
FDA 483 Rechon Life Science AB, Limhamn | 2014
Out-of-stock
Issued on: Mar 21, 2014
Human Drug Form 483
FDA 483 Rechon Life Science AB, Limhamn | 2011
Out-of-stock
Issued on: Sep 16, 2011
Human Drug Form 483
FDA 483 Rechon Life Science AB, Limhamn | 2008
Out-of-stock
Issued on: Apr 8, 2008
Human Drug Form 483
FDA 483 Rechon Life Science AB, Limhamn | 2004
Out-of-stock
Issued on: Mar 18, 2004
Human Drug Form 483
FDA 483 Rechon Life Science AB, Limhamn | 2001
Out-of-stock
Issued on: May 23, 2001
Human Drug Form 483
FDA Investigators(12)
- Lisa L. Flores, FDA Investigator
- Monica E. Murie, FDA Investigator
- MRA DavisM, FDA Investigator
- Frederick Razzaghi, FDA Investigator
- Akbar J. Zaidi, FDA Investigator
- Jose A. Cruz Gonzalez, FDA Investigator
- Cruz Gonzalez, Jose A, FDA Investigator
- Russell J. Glapion, FDA Investigator
- Helen B. Ricalde, FDA Investigator
- Tiffani D. Wilson, FDA Investigator
- Thomas J. Arista, FDA Investigator
- David M. Beltran, FDA Investigator