Home / Inspections / 953742

FDA Inspection 953742 — DLC Laboratories, Inc

DLC Laboratories, Inc — FEI 2020223

The FDA completed an inspection of DLC Laboratories, Inc on December 11, 2015 in Paramount, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
December 11, 2015
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Paramount, CA (United States)

Facility

Other inspections at this facility

  • 1259646 (VAI Fri Jan 31 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1113363 (VAI Thu Dec 12 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1046262 (VAI Fri Mar 30 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 780591 (VAI Thu May 03 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 737453 (VAI Wed Aug 03 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources