Suppliers / GE Healthcare Inc. (Medi-Physics, Inc. dba GE Healthcare)

GE Healthcare Inc. (Medi-Physics, Inc. dba GE Healthcare)

United States Updated 9 July 2026

The public registers hold a second record for GE Healthcare Inc. (Medi-Physics, Inc. dba GE Healthcare). The fuller profile, with 13 active US DMFs and 4 valid CEPs, is at GE Healthcare. Figures on this page cover only this record.

GE Healthcare Inc. (Medi-Physics, Inc. dba GE Healthcare) is a finished-dose manufacturer based in United States. It appears in 201 regulatory filings across 21 regulators, without an active US DMF or CEP on file. Its filings concentrate with FAMHP (BE), INFARMED (PT) and SAHPRA (ZA). Its GMP standing is certified by EAEU_EEC, US FDA and NAFDAC (NG). Its most recent recorded inspection, by US FDA, closed on 19 September 2025 as NAI.

0
active US DMFs
0
valid CEPs
3
registered plants 1 with an FDA FEI number
201
filings across 21 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
Inspections
8 of 8 confirmed
EU GMP
1 of 1 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. FDA drug inspection classifications, read 4 May 2026. EudraGMDP (MIA + third-country GMP certs), read 4 May 2026.

Inspection history

  • 19 September 2025 NAI US FDA
  • 8 March 2024 VAI US FDA
  • 24 January 2020 NAI US FDA
  • 5 March 2015 NAI US FDA
  • 9 July 2013 NAI US FDA
  • 13 February 2012 NAI US FDA
  • 8 April 2010 VAI US FDA
  • 2 July 2009 NAI US FDA

NAI means no action indicated, VAI means voluntary action indicated, and OAI means official action indicated.

Registered plants

Site FDA FEI
SHANGHAI (XANGAI), China Not on file
OSLO, Norway Not on file
Arlington Heights, United States 1417338

Filings and GMP by regulator

Regulator Filings GMP certificates
FAMHP (BE) 59 None
INFARMED (PT) 30 None
SAHPRA (ZA) 21 None
NMRC (NA) 18 None
MPA (SE) 17 None
DPM (TN) 11 None
EAEU_EEC None 1
US FDA None 1
NAFDAC (NG) None 1

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Open risk flags

  • The most recent inspection outcome was NAI, on 19 September 2025.

Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability
EudraGMDP and national regulators
GMP certificates