EMPWR Netherlands BV
FDA import alert and refusal historyLeerdam, NetherlandsFEI 3004661553
As of October 26, 2026, EMPWR Netherlands BV is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on December 12, 2017, most often for fair packaging and labeling act (LABELING).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Snack foods not elsewhere mentioned, n.e.c. · LABELING
- Last warning letter
- None found
- Last inspection
- Classified NAI (No Action Indicated)
Every FDA record for EMPWR Netherlands BV
3 records, newest first. Each line links to the FDA page it came from.
Refusal charges, in plain English
- LABELING1 refused line
Fair Packaging and Labeling Act
The package appeared not to meet the Fair Packaging and Labeling Act because of the placement, form, or contents of a required label statement.
Questions about EMPWR Netherlands BV
- Is EMPWR Netherlands BV on an FDA import alert?
- No listing for EMPWR Netherlands BV appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Netherlands page.
- Has FDA refused shipments from EMPWR Netherlands BV?
- Yes. FDA refused 1 shipment line from EMPWR Netherlands BV on December 12, 2017. The most recent, on December 12, 2017, was snack foods not elsewhere mentioned, n.e.c., charged as LABELING (fair packaging and labeling act).
- Why did FDA refuse EMPWR Netherlands BV's shipments?
- The most frequent charge is LABELING (fair packaging and labeling act, 1 line).
- When was EMPWR Netherlands BV last inspected by FDA?
- FDA's most recent inspection of EMPWR Netherlands BV with a final classification is dated September 18, 2024 and was classified NAI (No Action Indicated).
- What is EMPWR Netherlands BV's FEI number?
- EMPWR Netherlands BV's FDA Establishment Identifier (FEI) is 3004661553.
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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.