FDA Warning Letter — Repro-Med Systems, Inc.

Case 478416 — FEI 1318360

The FDA took a Warning Letter action against Repro-Med Systems, Inc. on February 26, 2016 (Chester, NY). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Repro-Med Systems, Inc.
Date
February 26, 2016
Fiscal Year
2016
Product Type
Devices
Center
CDRH
Location
Chester, NY (United States)