FDA Warning Letter — Xephyr, LLC

Case 604588 — FEI 3013861086

The FDA took a Warning Letter action against Xephyr, LLC on Mar 6, 2020 (Atoka, OK). The action was issued by CDER and concerns drugs products.

Action Details

Facility
Xephyr, LLC
Date
Mar 6, 2020
Fiscal Year
2020
Product Type
Drugs
Center
CDER
Location
Atoka, OK (United States)

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