FDA Inspection 1320182 — Vektor Medical, Inc.

Vektor Medical, Inc. — FEI 3021016555

The FDA completed an inspection of Vektor Medical, Inc. on May 12, 2026 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
May 12, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
San Diego, CA (United States)