FDA Inspection 1006653 — Mubashir Mumtaz, MD

Mubashir Mumtaz, MD — FEI 3013193225

The FDA completed an inspection of Mubashir Mumtaz, MD on Mar 1, 2017 in Mechanicsburg, PA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Mar 1, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Mechanicsburg, PA (United States)

Additional Details

Clinical Investigator (CI)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.