FDA Inspection 998957 — Tulane-Lakeside Hospital Laboratory

Tulane-Lakeside Hospital Laboratory — FEI 3013360618

The FDA completed an inspection of Tulane-Lakeside Hospital Laboratory on Dec 5, 2016 in Metairie, LA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Dec 5, 2016
Fiscal Year
2017
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Metairie, LA (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.