Home / Compliance actions / 519531

FDA Warning Letter — VIOS

Case 519531 — FEI 3005186075

The FDA took a Warning Letter action against VIOS on July 6, 2017 (Crest Hill, IL). The action was issued by CBER and concerns biologics products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
VIOS
Date
July 6, 2017
Fiscal Year
2017
Product Type
Biologics
Center
CBER
Location
Crest Hill, IL (United States)

Facility

Recent inspections

  • 1218025 (NAI Thu Sep 14 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1043268 (NAI Thu Feb 15 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1003678 (OAI Fri Feb 03 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 886244 (NAI Wed Jul 02 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 732394 (NAI Tue Jun 28 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources