Suppliers / AVA

AVA

United States Updated 9 July 2026

AVA is an API manufacturer based in United States. It holds one active US drug master file and one valid CEP across a filed portfolio of 2 molecules. Its most recent recorded inspection, by US FDA, closed on 21 October 2025 as OAI.

1
active US DMFs
1
valid CEPs
1
registered plants 1 with an FDA FEI number
2
filings across 1 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
Inspections
4 of 4 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. FDA drug inspection classifications, read 4 May 2026.

Inspection history

  • 21 October 2025 OAI US FDA
  • 29 September 2021 VAI US FDA
  • 30 March 2016 VAI US FDA
  • 15 May 2013 VAI US FDA

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

Registered plants

Site FDA FEI
Willowbrook, United States 3008736380

What they file, and where

Molecule Regulators Docs
Chlorhexidine US FDA 1
Chlorhexidine Digluconate EDQM 1

Also appears on these molecule pages

Chlorhexidine API

Filings and GMP by regulator

Regulator Filings GMP certificates
US FDA 2 None

Questions about AVA

Does AVA hold a US DMF or a CEP?
AVA holds 1 active US drug master file and 1 valid CEP. A drug master file is a submission to the FDA describing how an ingredient is made; a CEP is the EDQM's certificate that the substance meets its European Pharmacopoeia monograph. Both are filings rather than approvals.
Is AVA FDA-registered?
One site operated by AVA 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 AVA's last inspection go?
The most recent inspection on record closed on 21 October 2025 as OAI (Official Action Indicated, the worst classification: objectionable conditions were found and regulatory action was warranted). 4 inspections are on file, of which 1 closed as OAI.
Where does AVA manufacture?
1 registered site is on record, in United States (Willowbrook). Every site is listed on this page with the register it came from.
What does AVA make?
2 molecules are on record against AVA, including Chlorhexidine and Chlorhexidine Digluconate. Each links through to that molecule's full manufacturer list.
Where does AVA file?
Filings are on record with US FDA, 2 in total.

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 OAI, on 21 October 2025.

Comparable suppliers

Cadila Pharmaceuticals shares 1 molecule Medichem shares 1 molecule Far Specialty Products Inc Dba Far Chemical shares 1 molecule Jinzhou Jiutai Pharmaceutical shares 1 molecule Rn Laboratories shares 1 molecule

Ranked by shared active ingredients where we have them, otherwise by country and comparable credentials.

Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability