FDA Inspection 1076017 — Jennifer Keiser, M.D.

Jennifer Keiser, M.D. — FEI 3014711441

The FDA completed an inspection of Jennifer Keiser, M.D. on Dec 5, 2018 in Basel. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Dec 5, 2018
Fiscal Year
2019
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Basel (Switzerland)

Additional Details

Clinical Investigator (CI)

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