FDA Inspection 788873 — Guntur, Dr Vamsi

Guntur, Dr Vamsi — FEI 3009442585

The FDA completed an inspection of Guntur, Dr Vamsi on Jun 21, 2012 in Columbia, MO. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jun 21, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Columbia, MO (United States)

Additional Details

Clinical Investigator (CI)