FDA Inspection 1024855 — Melinta Therapeutics, Inc.

Melinta Therapeutics, Inc. — FEI 3012876740

The FDA completed an inspection of Melinta Therapeutics, Inc. on April 14, 2017 in Lincolnshire, IL. 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
April 14, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Lincolnshire, IL (United States)

Additional Details

Sponsor, Contract Research Organization