FDA Inspection 1000025 — Mobilab, Inc.

Mobilab, Inc. — FEI 1484171

The FDA completed an inspection of Mobilab, Inc. on Jan 25, 2017 in Peoria, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jan 25, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Peoria, IL (United States)