M.M. Enterprise
FDA import alert and refusal historyBorsad, IndiaFEI 3004672062
As of October 26, 2026, M.M. Enterprise (Borsad, India) is on the red list of FDA Import Alert 99-21 (Foods with undeclared added sulfiting agents) for mango bars (aam papad), published by FDA on September 29, 2011, is also listed on Import Alert 45-02 (red list) and Import Alert 99-19 (red list), and has no FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for M.M. Enterprise
3 records, newest first. Each line links to the FDA page it came from.
2011
- Import alert listingListed on Import Alert 99-21red listMango Bars (Aam Papad)Source
2009
- Import alert listingListed on Import Alert 45-02red listSoft Drink, Citrus Fruit Flavored, Carbonated; Soft Drink, Imitation Fruit Flavored, Carbonated; Soft Drink, Subtropical or Tropical Fruit Flavored, Carbonated; Carbonated Soft Drink, N.E.C.; Soft Drinks and Waters Not Mentioned Elsewhere, N.E.C.Source
- Import alert listingListed on Import Alert 99-19red listChilli Powder (aka chilly powder); coriander powder; cumin powder; Turmaric PowderSource
Questions about M.M. Enterprise
- Is M.M. Enterprise on an FDA import alert?
- Yes. As of October 26, 2026, M.M. Enterprise is on the red list of FDA Import Alert 99-21, “Foods with undeclared added sulfiting agents”, for mango bars (aam papad); FDA published the listing on September 29, 2011.
- Has FDA refused shipments from M.M. Enterprise?
- No FDA import refusals for M.M. Enterprise appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is M.M. Enterprise's FEI number?
- M.M. Enterprise's FDA Establishment Identifier (FEI) is 3004672062.
- Can shipments from M.M. Enterprise still enter the U.S.?
- Shipments of mango bars (aam papad) from M.M. Enterprise can be detained without physical examination under Import Alert 99-21; 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.