FDA Warning Letter — Manhattan Regenerative Medicine Medical Group

Case 483320 — FEI 3011770053

The FDA took a Warning Letter action against Manhattan Regenerative Medicine Medical Group on December 30, 2015 (New York, NY). The action was issued by CBER and concerns biologics products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
Manhattan Regenerative Medicine Medical Group
Date
December 30, 2015
Fiscal Year
2016
Product Type
Biologics
Center
CBER
Location
New York, NY (United States)