FDA Inspection 1016850 — Biolog, Inc.

Biolog, Inc. — FEI 3005786028

The FDA completed an inspection of Biolog, Inc. on Mar 21, 2017 in Newark, DE. 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
Mar 21, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Newark, DE (United States)