FDA Inspection 1018976 — Michael Schmitt, M.D.

Michael Schmitt, M.D. — FEI 3013411101

The FDA completed an inspection of Michael Schmitt, M.D. on Jun 23, 2017 in Heidelberg. 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
Jun 23, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Heidelberg (Germany)

Additional details

Clinical Investigator (CI)

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