FDA Inspection 1019525 — Rundback, John H., M.D
The FDA completed an inspection of Rundback, John H., M.D on June 22, 2017 in Teaneck, NJ. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- June 22, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- Teaneck, NJ (United States)
Additional Details
Clinical Investigator (CI)