FDA Inspection 1194330 — Nomax, Inc.

Nomax, Inc. — FEI 1937310

The FDA completed an inspection of Nomax, Inc. on December 2, 2022 in Saint Louis, MO. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
December 2, 2022
Fiscal Year
2023
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Saint Louis, MO (United States)