Qualitech Pharma Co., Ltd. - Shiga Plant
FDA import alert and refusal historyYasu, JapanFEI 3004392271
As of October 26, 2026, Qualitech Pharma Co., Ltd. - Shiga Plant has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on July 31, 2017, was classified VAI (Voluntary 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 VAI (Voluntary Action Indicated)
Every FDA record for Qualitech Pharma Co., Ltd. - Shiga Plant
2 records, newest first. Each line links to the FDA page it came from.
Questions about Qualitech Pharma Co., Ltd. - Shiga Plant
- Is Qualitech Pharma Co., Ltd. - Shiga Plant on an FDA import alert?
- No listing for Qualitech Pharma Co., Ltd. - Shiga Plant appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Japan page.
- Has FDA refused shipments from Qualitech Pharma Co., Ltd. - Shiga Plant?
- No FDA import refusals for Qualitech Pharma Co., Ltd. - Shiga Plant appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Qualitech Pharma Co., Ltd. - Shiga Plant last inspected by FDA?
- FDA's most recent inspection of Qualitech Pharma Co., Ltd. - Shiga Plant with a final classification is dated July 31, 2017 and was classified VAI (Voluntary Action Indicated).
- What is Qualitech Pharma Co., Ltd. - Shiga Plant's FEI number?
- Qualitech Pharma Co., Ltd. - Shiga Plant's FDA Establishment Identifier (FEI) is 3004392271.
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