Site records / India / FEI 3006744199
Makson Health Care Private LimitedSangareddy
FDA-registered drug establishment in Sangareddy: analysis, label, manufacture, pack. Registration valid to 31 Dec 2026. Record as observed 27 Sep 2026.
- Inspections posted
- 1
- Last inspection
- Sep 2022 · VAI
- Warning letters to this FEI
- 0
- Import alerts at this address
- 1
- US border refusals, 2 years
- 9
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.
- 29 Sep 2022VAI · Voluntary Action IndicatedDrug Quality Assurance · 7 citations posted
Warning letters and compliance actions
No FDA compliance action recorded against this FEI or letter to its name.
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.
- 29 May 2014Import alert 66-41 · Published address is this site SourceDetention Without Physical Examination of Unapproved New Drugs Promoted In The U.S.Published address: 182 - 183 Gummadidala Mandal , Survey , Annaram, Telangana INDIA
Registration
- FEI
- 3006744199
- DUNS
- 854279690
- Registered as
- MAKSON HEALTH CARE PRIVATE LIMITED
- Registrant
- MAKSON HEALTH CARE PRIVATE LIMITED
- Address
- Survey no: 182-183, Annaram Village, Gummadidala Mandal,, Sangareddy, 502313, India (IND)
- Operations
- ANALYSIS, LABEL, MANUFACTURE, PACK
- 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.