FDA Warning Letter — Wuhan Chinese Moxibustion Technology Dev. Co., Ltd.

Case 537648 — FEI 3004859058

The FDA took a Warning Letter action against Wuhan Chinese Moxibustion Technology Dev. Co., Ltd. on December 18, 2017 (Wuhan, China). The action was issued by CDER and concerns drugs products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
Wuhan Chinese Moxibustion Technology Dev. Co., Ltd.
Date
December 18, 2017
Fiscal Year
2018
Product Type
Drugs
Center
CDER
Location
Wuhan (China)