FDA Inspection 1037071 — Alan R. Schwartz, MD

Alan R. Schwartz, MD — FEI 3013769546

The FDA completed an inspection of Alan R. Schwartz, MD on December 5, 2017 in Baltimore, MD. 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
December 5, 2017
Fiscal Year
2018
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Baltimore, MD (United States)

Additional Details

Clinical Investigator (CI)