Is VISPAK d.d. on an FDA import alert?

No listing for VISPAK d.d. appears in the FDA import alerts SupplierRadar checked on October 25, 2026. Country-wide alerts may still apply to its products; see the Bosnia and Herzegovina page.

Has FDA refused shipments from VISPAK d.d.?

Yes. FDA refused 7 shipment lines from VISPAK d.d. on January 30, 2020. The most recent, on January 30, 2020, was cucumbers, with sauce, charged as NEEDS FCE (processor not registered for canned or acidified foods).

Why did FDA refuse VISPAK d.d.'s shipments?

The most frequent charges are NEEDS FCE (processor not registered for canned or acidified foods, 7 lines) and NO PROCESS (no scheduled process filed, 7 lines).

When was VISPAK d.d. last inspected by FDA?

FDA's most recent inspection of VISPAK d.d. with a final classification is dated March 5, 2024 and was classified NAI (No Action Indicated).

What is VISPAK d.d.'s FEI number?

VISPAK d.d.'s FDA Establishment Identifier (FEI) is 3003003576.

VISPAK d.d.

FDA import alert and refusal historyVisoko, Bosnia and HerzegovinaFEI 3003003576

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As of October 25, 2026, VISPAK d.d. is not on any FDA import alert in SupplierRadar's records; FDA refused 7 of its shipment lines on January 30, 2020, most often for processor not registered for canned or acidified foods (NEEDS FCE).

Data from FDA public records, last checked October 25, 2026. Request a correction

Current status

Import alerts: Not listed
Last import refusal: Jan 30, 2020Cucumbers, with sauce · NEEDS FCE
Last warning letter: None found
Last inspection: Mar 5, 2024Classified NAI (No Action Indicated)

Every FDA record for VISPAK d.d.

8 records, newest first. Each line links to the FDA page it came from.

2024

Mar 5, 2024Inspection
Inspection classified NAI (No Action Indicated)Foodborne Biological Hazards
Source

2020

Jan 30, 2020Import refusal
Refused, 7 lines in one entry: Cucumbers, with sauce; Pepper, sweet, with sauce and 2 moreNEEDS FCENO PROCESSEntry 164-0281227-1Show 7 linesHide lines
- Refused, Cucumbers, with sauceNEEDS FCE NO PROCESSEntry 164-0281227-1Source
- Refused, Pepper, sweet, with sauceNEEDS FCE NO PROCESSEntry 164-0281227-1Source
- Refused, Pepper, sweet, with sauceNEEDS FCE NO PROCESSEntry 164-0281227-1Source
- Refused, Pepper, sweet, with sauceNEEDS FCE NO PROCESSEntry 164-0281227-1Source
- Refused, Pimiento pepper, dried or pasteNEEDS FCE NO PROCESSEntry 164-0281227-1Source
- Refused, Beet tops, with sauceNEEDS FCE NO PROCESSEntry 164-0281227-1Source
- Refused, Pepper, sweet, with sauceNEEDS FCE NO PROCESSEntry 164-0281227-1Source
Source

Refusal charges, in plain English

NEEDS FCE7 refused lines
Processor not registered for canned or acidified foods
The manufacturer appeared not to be registered with FDA as a low-acid canned food or acidified food processor, as 21 CFR 108.25 and 108.35 require.
NO PROCESS7 refused lines
No scheduled process filed
The manufacturer appeared not to have filed a scheduled process with FDA, which 21 CFR Part 108 requires for low-acid canned and acidified foods, so the product is treated as made under insanitary conditions.

Questions about VISPAK d.d.

Is VISPAK d.d. on an FDA import alert?: No listing for VISPAK d.d. appears in the FDA import alerts SupplierRadar checked on October 25, 2026. Country-wide alerts may still apply to its products; see the Bosnia and Herzegovina page.
Has FDA refused shipments from VISPAK d.d.?: Yes. FDA refused 7 shipment lines from VISPAK d.d. on January 30, 2020. The most recent, on January 30, 2020, was cucumbers, with sauce, charged as NEEDS FCE (processor not registered for canned or acidified foods).
Why did FDA refuse VISPAK d.d.'s shipments?: The most frequent charges are NEEDS FCE (processor not registered for canned or acidified foods, 7 lines) and NO PROCESS (no scheduled process filed, 7 lines).
When was VISPAK d.d. last inspected by FDA?: FDA's most recent inspection of VISPAK d.d. with a final classification is dated March 5, 2024 and was classified NAI (No Action Indicated).
What is VISPAK d.d.'s FEI number?: VISPAK d.d.'s FDA Establishment Identifier (FEI) is 3003003576.

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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.