Heinrich Klenk Gmbh
FDA import alert and refusal historySchwebheim, GermanyFEI 1000379630
As of October 26, 2026, Heinrich Klenk Gmbh has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on December 12, 2018, was classified NAI (No Action Indicated).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified NAI (No Action Indicated)
Every FDA record for Heinrich Klenk Gmbh
2 records, newest first. Each line links to the FDA page it came from.
Questions about Heinrich Klenk Gmbh
- Is Heinrich Klenk Gmbh on an FDA import alert?
- No listing for Heinrich Klenk Gmbh appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Germany page.
- Has FDA refused shipments from Heinrich Klenk Gmbh?
- No FDA import refusals for Heinrich Klenk Gmbh appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Heinrich Klenk Gmbh last inspected by FDA?
- FDA's most recent inspection of Heinrich Klenk Gmbh with a final classification is dated December 12, 2018 and was classified NAI (No Action Indicated).
- What is Heinrich Klenk Gmbh's FEI number?
- Heinrich Klenk Gmbh's FDA Establishment Identifier (FEI) is 1000379630.
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