FDA Inspection 802889 — Aji, Janah, M.D.
The FDA completed an inspection of Aji, Janah, M.D. on October 19, 2012 in Camden, NJ. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- October 19, 2012
- Fiscal Year
- 2013
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- Camden, NJ (United States)
Additional Details
Clinical Investigator (CI)