FDA Inspection 1064850 — Mikart LLC

Mikart LLC — FEI 1050658

The FDA completed an inspection of Mikart LLC on August 23, 2018 in Atlanta, GA. 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
August 23, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Atlanta, GA (United States)

Additional Details

Postmarket Adverse Drug Experience (PADE)