FDA Inspection 1028545 — Navidea Biopharmaceuticals Inc
The FDA completed an inspection of Navidea Biopharmaceuticals Inc on August 11, 2017 in Dublin, OH. 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 11, 2017
- Fiscal Year
- 2017
- Product Type
- Drugs
- Project Area
- Bioresearch Monitoring
- Location
- Dublin, OH (United States)
Additional Details
Postmarket Adverse Drug Experience (PADE)