FDA Inspection 948313 — Lilly Del Caribe, Inc.

Lilly Del Caribe, Inc. — FEI 3005303436

The FDA completed an inspection of Lilly Del Caribe, Inc. on Nov 10, 2015 in Guayama, PR. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Nov 10, 2015
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Guayama, PR (United States)

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