FDA Inspection 715719 — Larken Laboratories, Inc.

Larken Laboratories, Inc. — FEI 3005966786

The FDA completed an inspection of Larken Laboratories, Inc. on March 3, 2011 in Canton, MS. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
March 3, 2011
Fiscal Year
2011
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Canton, MS (United States)