FDA Warning Letter — Diasol Inc

Case 535886 — FEI 3009491770

The FDA took a Warning Letter action against Diasol Inc on September 28, 2017 (Phillipsburg, NJ). The action was issued by CDRH and concerns devices products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
Diasol Inc
Date
September 28, 2017
Fiscal Year
2017
Product Type
Devices
Center
CDRH
Location
Phillipsburg, NJ (United States)