FDA Warning Letter — Nitrox, Inc.

Case 109051 — FEI 1000105891

The FDA took a Warning Letter action against Nitrox, Inc. on July 26, 2010 (Lynnwood, WA). The action was issued by CDER and concerns drugs products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
Nitrox, Inc.
Date
July 26, 2010
Fiscal Year
2010
Product Type
Drugs
Center
CDER
Location
Lynnwood, WA (United States)