Site records / Rajasthan / FEI 3015794560
Macsen DrugsUdaipur, Rajasthan
FDA-registered drug establishment in Udaipur, Rajasthan: api manufacture. Registration valid to 31 Dec 2026. Record as observed 27 Sep 2026.
- Inspections posted
- 1
- Last inspection
- Sep 2024 · OAI
- Warning letters to this FEI
- 1
- Import alerts at this address
- 1
- US border refusals, 2 years
- 2
This site, graded.
Every fact sourced.
- A grade from A to E on a registered ten-factor rubric, with the fact behind every factor
- Every posted FDA citation, sorted into failure categories and set against Indian drug inspections
- Warning-letter violations, numbered and labelled
- Import-alert history rebuilt from the archive, each listing checked against this address
- Border refusals by product, and the company's other sites, each graded
- A hash of every source read, so the PDF can be checked against the record
On 2022–26 inspections the rubric never saw, grade E sites were classified OAI 26.5% of the time and grade A sites 4.0%.
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Inspections
1 FDA inspection of this FEI, by end date; 1 with a posted classification.
- 6 Sep 2024OAI · Official Action IndicatedDrug Quality Assurance · no citations posted
Warning letters and compliance actions
- 5 Mar 2025Warning Letter · CDER SourceCGMP/Finished Pharmaceuticals/Adulterated
Import alerts in force
Import-alert pages list a firm name and an address, never an FEI. Each listing under this firm's name is shown with the address FDA published and whether it is this site's.
- 12 Feb 2016Import alert 66-66 · Published address is this site SourcePublished address: Ambamata Ki Ghati , Village Titerdi , Tehsil Girwa, Udaipur, Rajasthan INDIA
Registration
- FEI
- 3015794560
- DUNS
- 675486516
- Registered as
- MACSEN DRUGS
- Registrant
- MACSEN DRUGS
- Address
- F-261, 262, 263 RIICO Industrial Area Gudli, Tehsil Mavli,, Udaipur, Rajasthan 313024, India (IND)
- Operations
- API MANUFACTURE
- Registration expires
- 31 Dec 2026
Sources: FDA drug establishment registrations, FDA Data Dashboard inspections and compliance actions, import-alert pages, warning letters, import refusals and the FDA reading room, as held in Counterfoil's point-in-time corpus. No matched action does not establish compliance, and FDA registration is not FDA approval. Sources and coverage.