FDA Warning Letter — Robert J. Hayashi, MD

Case 654873 — FEI 3022205731

The FDA took a Warning Letter action against Robert J. Hayashi, MD on Mar 14, 2023 (Saint Louis, MO). The action was issued by CDER and concerns drugs products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
Robert J. Hayashi, MD
Date
Mar 14, 2023
Fiscal Year
2023
Product Type
Drugs
Center
CDER
Location
Saint Louis, MO (United States)

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