FDA Inspection 1103244 — Robert Puchalski MD

Robert Puchalski MD — FEI 3013341629

The FDA completed an inspection of Robert Puchalski MD on September 4, 2019 in Lugoff, SC. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
September 4, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Lugoff, SC (United States)

Additional Details

Clinical Investigator (CI)