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FDA Warning Letter — Melanie M Hoppers, MD

Case 671684 — FEI 3023878838

The FDA took a Warning Letter action against Melanie M Hoppers, MD on Nov 8, 2023 (Jackson, TN). The action was issued by CDER and concerns drugs products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
Melanie M Hoppers, MD
Date
Nov 8, 2023
Fiscal Year
2024
Product Type
Drugs
Center
CDER
Location
Jackson, TN (United States)

Facility

Recent inspections

FDA data resources

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