FDA Inspection 1267160 — VLV Associates, Inc.

VLV Associates, Inc. — FEI 2245539

The FDA completed an inspection of VLV Associates, Inc. on March 25, 2025 in Whippany, NJ. 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 25, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Whippany, NJ (United States)