Suppliers / Teyro Labs

Teyro Labs

India 191 employees 2 duplicate records merged Updated 9 July 2026

Teyro Labs is a finished-dose manufacturer based in India. It appears in 5 regulatory filings across 1 regulator, without an active US DMF or CEP on file. Its GMP standing is certified by CDSCO (India), US FDA and EMA. Its most recent recorded inspection, by US FDA, closed on 12 November 2025 as VAI.

0
active US DMFs
0
valid CEPs
4
registered plants 1 with an FDA FEI number
5
filings across 1 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
Inspections
1 of 1 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

  • 12 November 2025 VAI US FDA

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

Registered plants

Site FDA FEI
kancheepuram 601 301, India Not on file
Kanchipuram District, India 3021389808
Chennai, India Not on file
Kancheepuram, India Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
US FDA 5 1
CDSCO (India) None 2
EMA None 1

Questions about Teyro Labs

Does Teyro Labs hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Teyro Labs. It does have 5 filings with one regulator, so it is registered, just not with the two strong registers buyers usually screen on.
Is Teyro Labs FDA-registered?
One site operated by Teyro Labs 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 Teyro Labs's last inspection go?
The most recent inspection on record closed on 12 November 2025 as VAI (Voluntary Action Indicated: issues were found but did not warrant regulatory action). 1 inspection is on file.
Where does Teyro Labs manufacture?
4 registered sites are on record, in India (Kancheepuram 601 301, Kanchipuram District and Chennai among others). Every site is listed on this page with the register it came from.
Which regulators recognise Teyro Labs's GMP?
Current GMP certificates are on record from CDSCO (India), US FDA and EMA. 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 12 November 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