Suppliers / Meridian Medical Technologies

Meridian Medical Technologies

United States Updated 9 July 2026

Meridian Medical Technologies is a finished-dose manufacturer based in United States. It appears in 9 regulatory filings across 2 regulators, without an active US DMF or CEP on file. Its filings concentrate with US FDA and NPRA (MY). Its GMP standing is certified by US FDA. Its most recent recorded inspection, by US FDA, closed on 5 June 2024 as VAI.

0
active US DMFs
0
valid CEPs
2
registered plants 2 with an FDA FEI number
9
filings across 2 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
2 of 2 confirmed
Inspections
8 of 8 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. FDA drug inspection classifications, read 4 May 2026.

Inspection history

  • 5 June 2024 VAI US FDA
  • 21 December 2019 OAI US FDA
  • 24 March 2017 OAI US FDA
  • 23 March 2015 VAI US FDA
  • 25 November 2014 OAI US FDA
  • 21 February 2014 OAI US FDA
  • 9 October 2013 OAI US FDA
  • 29 April 2013 OAI US FDA

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

Registered plants

Site FDA FEI
St. Louis, United States 1950222
Bridgeton, United States 3033729014

Filings and GMP by regulator

Regulator Filings GMP certificates
US FDA 7 1
NPRA (MY) 2 None

Questions about Meridian Medical Technologies

Does Meridian Medical Technologies hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Meridian Medical Technologies. It does have 9 filings with 2 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Is Meridian Medical Technologies FDA-registered?
2 sites operated by Meridian Medical Technologies carry an FDA establishment identifier (FEI), which means they are registered with the FDA as a drug establishment. Registration is not the same as approval or inspection clearance.
How did Meridian Medical Technologies's last inspection go?
The most recent inspection on record closed on 5 June 2024 as VAI (Voluntary Action Indicated: issues were found but did not warrant regulatory action). 8 inspections are on file, of which 6 closed as OAI.
Where does Meridian Medical Technologies manufacture?
2 registered sites are on record, in United States (St. Louis and Bridgeton). Every site is listed on this page with the register it came from.
Which regulators recognise Meridian Medical Technologies's GMP?
Current GMP certificates are on record from US FDA. GMP recognition covers the manufacturing site, separately from any filing on the substance itself.

Answered from this company's own record. Where a register holds nothing, the question is not asked rather than answered with a zero. How we count our figures.

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Open risk flags

  • The most recent inspection outcome was VAI, on 5 June 2024.

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Sources on this page

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