Suppliers / Armstrong Pharmaceuticals

Armstrong Pharmaceuticals

United States 44 employees Updated 9 July 2026

Armstrong Pharmaceuticals is a finished-dose manufacturer based in United States. It appears in 3 regulatory filings across 1 regulator, without an active US DMF or CEP on file. Its GMP standing is certified by US FDA. Its most recent recorded inspection, by US FDA, closed on 19 July 2024 as VAI.

0
active US DMFs
0
valid CEPs
1
registered plants 1 with an FDA FEI number
3
filings across 1 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
Inspections
8 of 8 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. FDA drug inspection classifications, read 4 May 2026.

Inspection history

  • 19 July 2024 VAI US FDA
  • 14 July 2021 NAI US FDA
  • 3 April 2014 NAI US FDA
  • 5 October 2012 NAI US FDA
  • 14 June 2012 VAI US FDA
  • 11 December 2009 NAI US FDA
  • 13 November 2009 VAI US FDA
  • 29 September 2009 VAI US FDA

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

Registered plants

Site FDA FEI
Canton, United States 3007009553

Filings and GMP by regulator

Regulator Filings GMP certificates
US FDA 3 1

Questions about Armstrong Pharmaceuticals

Does Armstrong Pharmaceuticals hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Armstrong Pharmaceuticals. It does have 3 filings with one regulator, so it is registered, just not with the two strong registers buyers usually screen on.
Is Armstrong Pharmaceuticals FDA-registered?
One site operated by Armstrong Pharmaceuticals carries an FDA establishment identifier (FEI), which means it is registered with the FDA as a drug establishment. Registration is not the same as approval or inspection clearance.
How did Armstrong Pharmaceuticals's last inspection go?
The most recent inspection on record closed on 19 July 2024 as VAI (Voluntary Action Indicated: issues were found but did not warrant regulatory action). 8 inspections are on file.
Where does Armstrong Pharmaceuticals manufacture?
1 registered site is on record, in United States (Canton). Every site is listed on this page with the register it came from.
Which regulators recognise Armstrong Pharmaceuticals'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 19 July 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