FDA Warning Letter — Nurettin Yagmur Bokurt

Case 495561 — FEI 3012264388

The FDA took a Warning Letter action against Nurettin Yagmur Bokurt on Jun 2, 2016 (Kadikoy, Turkey). The action was issued by CDER and concerns drugs products.

Action Details

Facility
Nurettin Yagmur Bokurt
Date
Jun 2, 2016
Fiscal Year
2016
Product Type
Drugs
Center
CDER
Location
Kadikoy (Turkey)

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