Klassik Foods Pvt. Ltd.
FDA import alert and refusal historyNashik, IndiaFEI 3003684351
As of October 26, 2026, Klassik Foods Pvt. Ltd. (Nashik, India) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for creme,plain cookie, biscuit and wafer; creme filled/iced cookie,biscuit,wafer; filled/iced cookies,biscuits and wafers, n.e.c., 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
- None on record
Every FDA record for Klassik Foods Pvt. Ltd.
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 45-02red listCreme,Plain Cookie, Biscuit and Wafer; Creme Filled/Iced Cookie,Biscuit,Wafer; Filled/Iced Cookies,Biscuits and Wafers, N.E.C.Source
Questions about Klassik Foods Pvt. Ltd.
- Is Klassik Foods Pvt. Ltd. on an FDA import alert?
- Yes. As of October 26, 2026, Klassik Foods Pvt. Ltd. is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for creme,plain cookie, biscuit and wafer; creme filled/iced cookie,biscuit,wafer; filled/iced cookies,biscuits and wafers, n.e.c.; FDA published the listing on September 18, 2009.
- Has FDA refused shipments from Klassik Foods Pvt. Ltd.?
- No FDA import refusals for Klassik Foods Pvt. Ltd. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Klassik Foods Pvt. Ltd.'s FEI number?
- Klassik Foods Pvt. Ltd.'s FDA Establishment Identifier (FEI) is 3003684351.
- Can shipments from Klassik Foods Pvt. Ltd. still enter the U.S.?
- Shipments of creme,plain cookie, biscuit and wafer; creme filled/iced cookie,biscuit,wafer; filled/iced cookies,biscuits and wafers, n.e.c. from Klassik Foods Pvt. 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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