Hebei Shengxue Dacheng Pharmaceutical Co., Ltd. Production No.2 Department
Hebei Shengxue Dacheng Pharmaceutical Co., Ltd. Production No.2 Department is a drug establishment in Shijiazhuang, China, registered with the US FDA under FEI 3005851696. Its registered operations are: Analytical testing, API manufacture, Labelling, Packaging, Particle size reduction. No EU or UK GMP certificate is matched to this site in our data; that is not evidence it has none. 1 EU GMP non-compliance statement is recorded.
Sources: FDA Drug Establishments Current Registration Site (checked 2 Nov 2026); EudraGMDP; MHRA GMDP. Methodology
Registered operations
Business operations this establishment declares in its FDA registration. Registration is not an approval and says nothing about EU or UK GMP status.
GMP documents matched to this site (0)
No EU or UK GMP document is matched to this site. Sites are matched by name and address, so an unmatched site may still hold a certificate; ask the company for it.
A GMP document is matched to this site when its address names the site's street and its city or postcode. In our latest internal review 59 of 60 sampled matches were the right site (not yet independently reviewed; measured match quality). Check the certificate's own address before relying on it. The three-year review window is the EMA guideline default after an inspection, not an official expiry date.
EU GMP non-compliance statements (1)
- Competent authority of Spain · 15 Jun 2023ES/099HV/25View on EudraGMDP
A non-compliance statement may since have been closed out; check the source record for its current status.
What this page does not show
- Which substances are made here: DMFs and CEPs are filed by organisations, not sites, so we do not link substances to this site.
- Capacity, scale, price or current availability: no regulator publishes these.
- FDA inspection classifications for this site, which are not yet linked.