FDA Inspection 673592 — Nomax, Inc.

Nomax, Inc. — FEI 1937310

The FDA completed an inspection of Nomax, Inc. on July 26, 2010 in Saint Louis, MO. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
July 26, 2010
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Saint Louis, MO (United States)