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FDA Inspection 1042698 — Michelle D. Ababa, MD

Michelle D. Ababa, MD — FEI 3013601029

The FDA completed an inspection of Michelle D. Ababa, MD on Oct 23, 2017 in Cypress, CA. 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
Oct 23, 2017
Fiscal Year
2018
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Cypress, CA (United States)

Additional Details

Clinical Investigator (CI)

Facility

FDA data resources

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