FDA Warning Letter — Asept Pak Inc.

Case 335838 — FEI 3007177643

The FDA took a Warning Letter action against Asept Pak Inc. on August 7, 2012 (Malone, 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
Asept Pak Inc.
Date
August 7, 2012
Fiscal Year
2012
Product Type
Devices
Center
CDRH
Location
Malone, NY (United States)