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FDA Inspection 780591 — DLC Laboratories, Inc

DLC Laboratories, Inc — FEI 2020223

The FDA completed an inspection of DLC Laboratories, Inc on May 3, 2012 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
May 3, 2012
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Paramount, CA (United States)

Facility

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FDA data resources