ZHEJIANG SKYHERB BIOTECHNOLOGY INC. FDA Record
ZHEJIANG SKYHERB BIOTECHNOLOGY INC. has 0 FDA recalls, 1 inspection, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "ZHEJIANG SKYHERB BIOTECHNOLOGY INC." is on file.
- Latest inspection
- Aug 20, 2019 · VAI
Summary
| Records | Count | Last refreshed | Source as of | Status |
|---|---|---|---|---|
| Recalls | 0 | Nov 8, 2026 | File dated Nov 3, 2026 | Current |
| 510(k) clearances | 0 | Nov 8, 2026 | File dated Nov 2, 2026 | Current |
| Inspections | 1 | Nov 14, 2026 | Newest record Nov 5, 2026 | Current |
| Compliance actions | 0 | Nov 2, 2026 | Newest record Oct 29, 2026 | Current |
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Recent FDA inspections
| Date | Site | Product | Classification | FEI |
|---|---|---|---|---|
| Aug 20, 2019 | Huzhou, China | Food/Cosmetics | Voluntary Action Indicated (VAI) | 3013253172 |
- NAI
- No objectionable conditions or practices were found during the inspection.
- VAI
- Objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action.
- OAI
- Regulatory and/or administrative actions are recommended.
FDA-inspected facilities
| Facility | Location | Inspections | Latest |
|---|---|---|---|
| FEI 3013253172 | Huzhou, China | 1 | Aug 20, 2019 |
ZHEJIANG SKYHERB BIOTECHNOLOGY INC. and the FDA: common questions
Has ZHEJIANG SKYHERB BIOTECHNOLOGY INC. received an FDA warning letter?
No FDA warning letter addressed to the name "ZHEJIANG SKYHERB BIOTECHNOLOGY INC." is on file. This answer covers that name only: letters addressed to a related company name or to one of its sites are listed on that name's or site's own page.
Has ZHEJIANG SKYHERB BIOTECHNOLOGY INC. received an FDA Form 483?
FDA has not published a Form 483 for "ZHEJIANG SKYHERB BIOTECHNOLOGY INC." in its reading room. FDA publishes some Form 483s, not all of them.
When did the FDA last inspect ZHEJIANG SKYHERB BIOTECHNOLOGY INC.?
The most recent FDA inspection on file ended Aug 20, 2019 at Huzhou, China and was classified VAI. FDA has 1 inspection of ZHEJIANG SKYHERB BIOTECHNOLOGY INC. on file.
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