Suppliers / Aaa Pharmaceuticals

Aaa Pharmaceuticals

United States Updated 9 July 2026

Aaa Pharmaceuticals is a finished-dose manufacturer based in United States. It appears in 10 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 28 March 2025 as VAI.

0
active US DMFs
0
valid CEPs
2
registered plants 2 with an FDA FEI number
10
filings across 1 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

  • 28 March 2025 VAI US FDA
  • 15 May 2024 VAI US FDA
  • 3 April 2019 VAI US FDA
  • 21 April 2016 NAI US FDA
  • 14 March 2014 VAI US FDA
  • 14 March 2014 NAI US FDA
  • 14 February 2013 NAI US FDA
  • 13 February 2013 NAI US FDA

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

Registered plants

Site FDA FEI
Lumberton, United States 3010027650
Paulsboro, United States 2246707

Filings and GMP by regulator

Regulator Filings GMP certificates
US FDA 10 2

Questions about Aaa Pharmaceuticals

Does Aaa Pharmaceuticals hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Aaa Pharmaceuticals. It does have 10 filings with one regulator, so it is registered, just not with the two strong registers buyers usually screen on.
Is Aaa Pharmaceuticals FDA-registered?
2 sites operated by Aaa Pharmaceuticals 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 Aaa Pharmaceuticals's last inspection go?
The most recent inspection on record closed on 28 March 2025 as VAI (Voluntary Action Indicated: issues were found but did not warrant regulatory action). 8 inspections are on file.
Where does Aaa Pharmaceuticals manufacture?
2 registered sites are on record, in United States (Lumberton and Paulsboro). Every site is listed on this page with the register it came from.
Which regulators recognise Aaa 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 28 March 2025.

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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