FDA Warning Letter — Robert J. Hayashi, MD

Case 654873 — FEI 3022205731

The FDA took a Warning Letter action against Robert J. Hayashi, MD on March 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
March 14, 2023
Fiscal Year
2023
Product Type
Drugs
Center
CDER
Location
Saint Louis, MO (United States)