FDA Inspection 1308722 — Peter R. Movilla, MD

Peter R. Movilla, MD — FEI 3042665385

The FDA completed an inspection of Peter R. Movilla, MD on March 19, 2026 in Newton Lower Falls, MA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
March 19, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Newton Lower Falls, MA (United States)

Additional Details

Clinical Investigator (CI)

Citations

IDCFRDescription
297421 CFR 812.110(b)Investigator non-compliance with agreement/plan/regulations