Pharmadass Limited
FDA import alert and refusal historyHarrow, United KingdomFEI 3004653190
As of October 26, 2026, Pharmadass Limited (Harrow, United Kingdom) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for ginseng extract; guaramax guarana capsules, published by FDA on September 18, 2009, and has no 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
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified NAI (No Action Indicated)
Every FDA record for Pharmadass Limited
2 records, newest first. Each line links to the FDA page it came from.
2011
- InspectionInspection classified NAI (No Action Indicated)Food Composition, Standards, Labeling and EconSource
2009
- Import alert listingListed on Import Alert 45-02red listGinseng Extract; Guaramax Guarana CapsulesSource
Questions about Pharmadass Limited
- Is Pharmadass Limited on an FDA import alert?
- Yes. As of October 26, 2026, Pharmadass Limited is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for ginseng extract; guaramax guarana capsules; FDA published the listing on September 18, 2009.
- Has FDA refused shipments from Pharmadass Limited?
- No FDA import refusals for Pharmadass Limited appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Pharmadass Limited last inspected by FDA?
- FDA's most recent inspection of Pharmadass Limited with a final classification is dated November 4, 2011 and was classified NAI (No Action Indicated).
- What is Pharmadass Limited's FEI number?
- Pharmadass Limited's FDA Establishment Identifier (FEI) is 3004653190.
- Can shipments from Pharmadass Limited still enter the U.S.?
- Shipments of ginseng extract; guaramax guarana capsules from Pharmadass Limited 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.