LLC Pharmacor Production
FDA import alert and refusal historySankt-Peterburg, RussiaFEI 3029360124
Recorded by FDA as LLC PHARMACOR PRODUCTION
As of October 26, 2026, LLC Pharmacor Production (Sankt-Peterburg, Russia) is on the red list of FDA Import Alert 99-39 (Imported foods that appear to be misbranded) for dietary supplement vladonix, published by FDA on February 23, 2024, and has 2 FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 99-39 · red list
- Last import refusal
- Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c. · INCONSPICU
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for LLC Pharmacor Production
3 records, newest first. Each line links to the FDA page it came from.
2026
- Import refusalRefused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.INCONSPICUNUTRIT LBLUNAPPROVEDEntry AEK-9263378-1Source
2024
- Import refusalRefused, Dietary conventional foods, n.e.c.LIST INGRELACKS FIRMNO ENGLISHNUTRIT LBLHEALTH CUNAPPROVEDEntry AEK-4374801-9Source
- Import alert listingListed on Import Alert 99-39red listDietary supplement vladonixSource
Refusal charges, in plain English
- NUTRIT LBL2 refused lines
Nutrition information missing from label
The label or labeling appeared not to carry the nutrition information that U.S. law requires for the food.
- 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.
- HEALTH C1 refused line
Unauthorized nutrient content or health claim
The label or labeling appeared to carry a nutrient content claim or health claim that is not authorized.
- INCONSPICU1 refused line
Required information not conspicuous
Information required on the label appeared not to be placed prominently or conspicuously enough to be read and understood by an ordinary consumer.
- LACKS FIRM1 refused line
Manufacturer name and address missing
The packaged product's label appeared not to show the name and place of business of the manufacturer, packer, or distributor.
- LIST INGRE1 refused line
Ingredients not listed
The product is made from two or more ingredients and the label appeared not to list the common or usual name of each one (or, for a juice beverage, the percentage of juice).
- NO ENGLISH1 refused line
Required label information not in English
Information that must appear on the label appeared not to be given in English, or not to be repeated in every language used on the label.
Questions about LLC Pharmacor Production
- Is LLC Pharmacor Production on an FDA import alert?
- Yes. As of October 26, 2026, LLC Pharmacor Production is on the red list of FDA Import Alert 99-39, “Imported foods that appear to be misbranded”, for dietary supplement vladonix; FDA published the listing on February 23, 2024.
- Has FDA refused shipments from LLC Pharmacor Production?
- Yes. FDA refused 2 shipment lines from LLC Pharmacor Production between March 6, 2024 and February 11, 2026. The most recent, on February 11, 2026, was vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c., charged as INCONSPICU (required information not conspicuous).
- Why did FDA refuse LLC Pharmacor Production's shipments?
- The most frequent charges are NUTRIT LBL (nutrition information missing from label, 2 lines) and UNAPPROVED (unapproved new drug, 2 lines).
- What is LLC Pharmacor Production's FEI number?
- LLC Pharmacor Production's FDA Establishment Identifier (FEI) is 3029360124.
- Can shipments from LLC Pharmacor Production still enter the U.S.?
- Shipments of dietary supplement vladonix from LLC Pharmacor Production can be detained without physical examination under Import Alert 99-39; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).
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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.