Suppliers / Aet Laboratories

Aet Laboratories

India Updated 9 July 2026

Aet Laboratories is a finished-dose manufacturer based in India. It appears in 15 regulatory filings across 2 regulators, without an active US DMF or CEP on file. Its filings concentrate with CDSCO (India) and JFDA (JO). Its GMP standing is certified by EMA and US FDA. Its most recent recorded inspection, by US FDA, closed on 7 February 2025 as VAI. Customs aggregates show $20.0M of exports covering 287 molecules to 22 destinations in 2025.

0
active US DMFs
0
valid CEPs
2
registered plants 1 with an FDA FEI number
15
filings across 2 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
Inspections
2 of 2 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

  • 7 February 2025 VAI US FDA
  • 20 September 2019 VAI US FDA

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

Registered plants

Site FDA FEI
Telangana State, United Arab Emirates Not on file
Sangareddy, India 3015218020

Filings and GMP by regulator

Regulator Filings GMP certificates
CDSCO (India) 12 None
JFDA (JO) 3 None
EMA None 1
US FDA None 1

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $3.1M 14
2025 Not reported $20.0M 22
2024 Not reported $56.4M 21
2023 Not reported $22.4M 14

Export figures are customs aggregates. We do not publish the identity of any buyer.

Comparing suppliers?

Choose your molecules and target markets. Aet Laboratories comes back tiered against every other supplier able to file there.

Start for free
No sales call.

Open risk flags

  • The most recent inspection outcome was VAI, on 7 February 2025.

Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability
EudraGMDP and national regulators
GMP certificates
Customs aggregates
Export values, molecule and destination counts