FDA Inspection 1073398 — Edmund Claxton, MD

Edmund Claxton, MD — FEI 3014737217

The FDA completed an inspection of Edmund Claxton, MD on Dec 4, 2018 in Lewiston, ME. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). 3 citations were issued during this inspection. Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Dec 4, 2018
Fiscal Year
2019
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Lewiston, ME (United States)

Additional Details

Clinical Investigator (CI)

Citations

IDCFRDescription
753021 CFR 312.62(b)Case history records- inadequate or inadequate
756021 CFR 312.60FD-1572, protocol compliance
766421 CFR 50.20Circumstances of obtaining consent

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