Pawan Kumar
FDA import alert and refusal historyNew Delhi, IndiaFEI 3017058078
Recorded by FDA as PAWAN KUMAR
As of October 26, 2026, Pawan Kumar is not on any FDA import alert in SupplierRadar's records; FDA refused 3 of its shipment lines on July 21, 2020, most often for unapproved new drug (UNAPPROVED).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Vitamin, n.e.c. · UNAPPROVED
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Pawan Kumar
3 records, newest first. Each line links to the FDA page it came from.
2020
- Import refusalSource
Refused, 3 lines in one entry: Vitamin, n.e.c.; Folic acid (vitamin) and 1 moreUNAPPROVEDEntry SCS-0888135-3Show 3 linesHide lines
- Refused, Vitamin, n.e.c.UNAPPROVEDEntry SCS-0888135-3Source
- Refused, Folic acid (vitamin)UNAPPROVEDEntry SCS-0888135-3Source
- Refused, Vitamin e (tocopherol)UNAPPROVEDEntry SCS-0888135-3Source
Refusal charges, in plain English
- UNAPPROVED3 refused lines
Unapproved new drug
The product appeared to be a new drug within the meaning of section 201(p) of the FD&C Act without an approved New Drug Application. FDA can apply this charge to a food or supplement whose labeling presents it for drug uses.
Questions about Pawan Kumar
- Is Pawan Kumar on an FDA import alert?
- No listing for Pawan Kumar appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the India page.
- Has FDA refused shipments from Pawan Kumar?
- Yes. FDA refused 3 shipment lines from Pawan Kumar on July 21, 2020. The most recent, on July 21, 2020, was vitamin, n.e.c., charged as UNAPPROVED (unapproved new drug).
- Why did FDA refuse Pawan Kumar's shipments?
- The most frequent charge is UNAPPROVED (unapproved new drug, 3 lines).
- What is Pawan Kumar's FEI number?
- Pawan Kumar's FDA Establishment Identifier (FEI) is 3017058078.
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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.