FDA Inspection 1234369 — Vektor Medical, Inc.

Vektor Medical, Inc. — FEI 3021016555

The FDA completed an inspection of Vektor Medical, Inc. on March 7, 2024 in San Diego, CA. 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
March 7, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
San Diego, CA (United States)

Additional Details

Sponsor, Contract Research Organization