Dr Ma's Laboratories, Inc.

9 records, newest first. Each line links to the FDA page it came from.

Refusal charges, in plain English

• SUPPL GMP4 refused lines

  Dietary supplement CGMP not met

  The product appeared to be a dietary supplement prepared, packed, or held under conditions that do not meet current good manufacturing practice (CGMP) regulations.

• 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.

• 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.

• NCONTACT1 refused line

  No U.S. adverse event contact on supplement label

  The dietary supplement label appeared not to show a U.S. address or phone number through which a serious adverse event can be reported.

• STD NAME1 refused line

  STD NAME

Questions about Dr Ma's Laboratories, Inc.

Is Dr Ma's Laboratories, Inc. on an FDA import alert?

Yes. As of October 26, 2026, Dr Ma's Laboratories, Inc. is on the red list of FDA Import Alert 99-39, “Imported foods that appear to be misbranded”, for living alchemy ashwagandha; lovita bee propolis liquid extract; FDA published the listing on March 27, 2025.

Has FDA refused shipments from Dr Ma's Laboratories, Inc.?

Yes. FDA refused 7 shipment lines from Dr Ma's Laboratories, Inc. between July 20, 2022 and July 10, 2026. The most recent, on July 10, 2026, was herbals & botanicals (not teas), n.e.c., charged as FILTHY (filthy, putrid or decomposed substance).

Why did FDA refuse Dr Ma's Laboratories, Inc.'s shipments?

The most frequent charges are SUPPL GMP (dietary supplement cgmp not met, 4 lines) and NUTRIT LBL (nutrition information missing from label, 2 lines).

When was Dr Ma's Laboratories, Inc. last inspected by FDA?

FDA's most recent inspection of Dr Ma's Laboratories, Inc. with a final classification is dated May 16, 2024 and was classified OAI (Official Action Indicated).

What is Dr Ma's Laboratories, Inc.'s FEI number?

Dr Ma's Laboratories, Inc.'s FDA Establishment Identifier (FEI) is 3015391683.

Can shipments from Dr Ma's Laboratories, Inc. still enter the U.S.?

Shipments of living alchemy ashwagandha; lovita bee propolis liquid extract from Dr Ma's Laboratories, Inc. 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).