Osotspa Public Company, Ltd.
FDA import alert and refusal historyBang Kapi, ThailandFEI 3004270719
As of October 26, 2026, Osotspa Public Company, Ltd. (Bang Kapi, Thailand) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for noncarbonated soft drink, n.e.c.; beverage base of non-fruit origin, liquid, n.e.c.; beverage base not mentioned elsewhere, n.e.c.; herbals & botanicals (not teas), n.e.c.; vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c., published by FDA on September 18, 2009, 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 45-02 · red list
- Last import refusal
- Tamarind, dried or paste · FILTHY
- Last warning letter
- None found
- Last inspection
- Classified NAI (No Action Indicated)
Every FDA record for Osotspa Public Company, Ltd.
4 records, newest first. Each line links to the FDA page it came from.
2026
2024
- Import refusalRefused, Noncarbonated soft drink, n.e.c.UNSAFE COLCOLOR LBLGEntry 9NK-0024436-6Source
2018
- InspectionInspection classified NAI (No Action Indicated)Foodborne Biological HazardsSource
2009
- Import alert listingListed on Import Alert 45-02red listNoncarbonated Soft Drink, N.E.C.; Beverage Base of Non-Fruit Origin, Liquid, N.E.C.; Beverage Base Not Mentioned Elsewhere, N.E.C.; Herbals & Botanicals (not Teas), N.E.C.; Vitamin, Mineral, Proteins and Unconventional Dietary Specialities For Humans and Animals, N.E.C.Source
Refusal charges, in plain English
- COLOR LBLG1 refused line
Artificial coloring not declared
The product appeared to contain an artificial coloring without labeling that states that fact.
- FILTHY1 refused line
Filthy, putrid or decomposed substance
The product appeared to consist in whole or in part of a filthy, putrid, or decomposed substance, or to be otherwise unfit for food.
- 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 Osotspa Public Company, Ltd.
- Is Osotspa Public Company, Ltd. on an FDA import alert?
- Yes. As of October 26, 2026, Osotspa Public Company, Ltd. is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for noncarbonated soft drink, n.e.c.; beverage base of non-fruit origin, liquid, n.e.c.; beverage base not mentioned elsewhere, n.e.c.; herbals & botanicals (not teas), n.e.c.; vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.; FDA published the listing on September 18, 2009.
- Has FDA refused shipments from Osotspa Public Company, Ltd.?
- Yes. FDA refused 2 shipment lines from Osotspa Public Company, Ltd. between May 8, 2024 and April 28, 2026. The most recent, on April 28, 2026, was tamarind, dried or paste, charged as FILTHY (filthy, putrid or decomposed substance).
- Why did FDA refuse Osotspa Public Company, Ltd.'s shipments?
- The most frequent charges are COLOR LBLG (artificial coloring not declared, 1 line) and FILTHY (filthy, putrid or decomposed substance, 1 line).
- When was Osotspa Public Company, Ltd. last inspected by FDA?
- FDA's most recent inspection of Osotspa Public Company, Ltd. with a final classification is dated May 22, 2018 and was classified NAI (No Action Indicated).
- What is Osotspa Public Company, Ltd.'s FEI number?
- Osotspa Public Company, Ltd.'s FDA Establishment Identifier (FEI) is 3004270719.
- Can shipments from Osotspa Public Company, Ltd. still enter the U.S.?
- Shipments of noncarbonated soft drink, n.e.c.; beverage base of non-fruit origin, liquid, n.e.c.; beverage base not mentioned elsewhere, n.e.c.; herbals & botanicals (not teas), n.e.c.; vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c. from Osotspa Public Company, Ltd. can be detained without physical examination under Import Alert 45-02; 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.