FDA Inspection 1263506 — Mariela Geneva Popova

Mariela Geneva Popova — FEI 3032968169

The FDA completed an inspection of Mariela Geneva Popova on Feb 27, 2025 in Plovdiv. 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
Feb 27, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Plovdiv (Bulgaria)

Additional Details

Clinical Investigator (CI)

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