FDA Inspection 1042561 — ARK-LA-TEX Fertility And Reproductive Medicine, PMC

ARK-LA-TEX Fertility And Reproductive Medicine, PMC — FEI 3010600107

The FDA completed an inspection of ARK-LA-TEX Fertility And Reproductive Medicine, PMC on Nov 30, 2017 in Shreveport, 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
Nov 30, 2017
Fiscal Year
2018
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Shreveport, LA (United States)

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