Alokozay Cola Production
FDA import alert and refusal historyKabul, AfghanistanFEI 3016752781
As of October 26, 2026, Alokozay Cola Production is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on November 23, 2022, most often for color additive unsafe under section 721 (UNSAFE COL).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Soft drink, imitation fruit flavored, carbonated · UNSAFE COL
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Alokozay Cola Production
1 record, newest first. Each line links to the FDA page it came from.
2022
- Import refusalRefused, Soft drink, imitation fruit flavored, carbonatedUNSAFE COLEntry 300-1172816-0Source
Refusal charges, in plain English
- UNSAFE COL1 refused line
Color additive unsafe under section 721
The product appeared to be, or to contain, a color additive that is unsafe within the meaning of section 721(a) of the FD&C Act, the section that governs which color additives may be used and how.
Questions about Alokozay Cola Production
- Is Alokozay Cola Production on an FDA import alert?
- No listing for Alokozay Cola Production appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Afghanistan page.
- Has FDA refused shipments from Alokozay Cola Production?
- Yes. FDA refused 1 shipment line from Alokozay Cola Production on November 23, 2022. The most recent, on November 23, 2022, was soft drink, imitation fruit flavored, carbonated, charged as UNSAFE COL (color additive unsafe under section 721).
- Why did FDA refuse Alokozay Cola Production's shipments?
- The most frequent charge is UNSAFE COL (color additive unsafe under section 721, 1 line).
- What is Alokozay Cola Production's FEI number?
- Alokozay Cola Production's FDA Establishment Identifier (FEI) is 3016752781.
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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.