Odessa factory of mineral water "Kuyalnik"
FDA import alert and refusal historyOdesa, UkraineFEI 3010011790
As of October 27, 2026, Odessa factory of mineral water "Kuyalnik" is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on July 24, 2017, 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
- Bottled spring or mineral water · UNAPPROVED
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Odessa factory of mineral water "Kuyalnik"
1 record, newest first. Each line links to the FDA page it came from.
2017
- Import refusalRefused, Bottled spring or mineral waterUNAPPROVEDEntry BQL-0050472-8Source
Refusal charges, in plain English
- UNAPPROVED1 refused line
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 Odessa factory of mineral water "Kuyalnik"
- Is Odessa factory of mineral water "Kuyalnik" on an FDA import alert?
- No listing for Odessa factory of mineral water "Kuyalnik" appears in the FDA import alerts SupplierRadar checked on October 27, 2026. Country-wide alerts may still apply to its products; see the Ukraine page.
- Has FDA refused shipments from Odessa factory of mineral water "Kuyalnik"?
- Yes. FDA refused 1 shipment line from Odessa factory of mineral water "Kuyalnik" on July 24, 2017. The most recent, on July 24, 2017, was bottled spring or mineral water, charged as UNAPPROVED (unapproved new drug).
- Why did FDA refuse Odessa factory of mineral water "Kuyalnik"'s shipments?
- The most frequent charge is UNAPPROVED (unapproved new drug, 1 line).
- What is Odessa factory of mineral water "Kuyalnik"'s FEI number?
- Odessa factory of mineral water "Kuyalnik"'s FDA Establishment Identifier (FEI) is 3010011790.
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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.