Khawaja Brothers
FDA import alert and refusal historySialkot, PakistanFEI 3011927161
As of October 26, 2026, Khawaja Brothers is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines on February 20, 2024, 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
- Herbals & botanical teas, n.e.c. · UNAPPROVED
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Khawaja Brothers
2 records, newest first. Each line links to the FDA page it came from.
2024
- Import refusalSource
Refused, 2 lines in one entry: Herbals & botanical teas, n.e.c.; Psyllium (fiber)UNAPPROVEDEntry KM6-3615223-3Show 2 linesHide lines
- Refused, Herbals & botanical teas, n.e.c.UNAPPROVEDEntry KM6-3615223-3Source
- Refused, Psyllium (fiber)UNAPPROVEDEntry KM6-3615223-3Source
Refusal charges, in plain English
- UNAPPROVED2 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 Khawaja Brothers
- Is Khawaja Brothers on an FDA import alert?
- No listing for Khawaja Brothers appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Pakistan page.
- Has FDA refused shipments from Khawaja Brothers?
- Yes. FDA refused 2 shipment lines from Khawaja Brothers on February 20, 2024. The most recent, on February 20, 2024, was herbals & botanical teas, n.e.c., charged as UNAPPROVED (unapproved new drug).
- Why did FDA refuse Khawaja Brothers's shipments?
- The most frequent charge is UNAPPROVED (unapproved new drug, 2 lines).
- What is Khawaja Brothers's FEI number?
- Khawaja Brothers's FDA Establishment Identifier (FEI) is 3011927161.
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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.