FDA Inspection 1059282 — VLV Associates, Inc.
The FDA completed an inspection of VLV Associates, Inc. on Jun 14, 2018 in Whippany, NJ. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection details
- Classification
- No Action Indicated (NAI)
- End Date
- Jun 14, 2018
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Whippany, NJ (United States)