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FDA Inspection 1097298 — Lilly del Caribe, Inc

Lilly del Caribe, Inc — FEI 2619243

The FDA completed an inspection of Lilly del Caribe, Inc on July 12, 2019 in Carolina, PR. 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
July 12, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Carolina, PR (United States)

Facility

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  • 1069938 (VAI Fri Sep 21 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1020761 (VAI Fri Jul 21 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 927312 (NAI Fri May 01 2015 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources