FDA Inspection 635938 — VLV Associates, Inc.

VLV Associates, Inc. — FEI 2245539

The FDA completed an inspection of VLV Associates, Inc. on Dec 23, 2009 in Whippany, NJ. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Dec 23, 2009
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Whippany, NJ (United States)

Citations

IDCFRDescription
369221 CFR 820.100(a)(4)CAPA verification/validation of corrective/preventive action

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.