Home / Inspections / 1059282

FDA Inspection 1059282 — VLV Associates, Inc.

VLV Associates, Inc. — FEI 2245539

The FDA completed an inspection of VLV Associates, Inc. on June 14, 2018 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
June 14, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Whippany, NJ (United States)

Facility

Other inspections at this facility

  • 1267160 (NAI Tue Mar 25 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1172618 (NAI Thu Jun 02 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 864983 (NAI Thu Jan 30 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 735402 (NAI Thu Jul 14 2011 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 635938 (NAI Wed Dec 23 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources