FDA Warning Letter — American Preclinical Services

Case 562382 — FEI 3005802236

The FDA took a Warning Letter action against American Preclinical Services on Feb 12, 2019 (Minneapolis, MN). The action was issued by CDRH and concerns devices products.

Action Details

Facility
American Preclinical Services
Date
Feb 12, 2019
Fiscal Year
2019
Product Type
Devices
Center
CDRH
Location
Minneapolis, MN (United States)