FDA Inspection 846219 — Kimberly-Clark Corp

Kimberly-Clark Corp — FEI 1031395

The FDA completed an inspection of Kimberly-Clark Corp on Aug 29, 2013 in Corinth, MS. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Aug 29, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Corinth, MS (United States)