# Qilu SYNVA Pharmaceutical Co. Ltd - Inspection Records

Source: https://www.keypedia.com/companies/qilu-synva-pharmaceutical-co-ltd/fda44d3b-5f42-4cde-9760-cf4147fc0ef8

> Inspection records and compliance data for Qilu SYNVA Pharmaceutical Co. Ltd in Dezhou, None. Access full analysis and detailed observations.

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## Details

- Name: Qilu SYNVA Pharmaceutical Co. Ltd
- FEI Number: 3006385404
- City: Dezhou
- State: None
- Country Name: China
- Address Line 1: 28 Licheng Ave, Linyi County
- Zip Code: None

## Related Documents

- [483 - Qilu SYNVA Pharmaceutical Co. Ltd - 2025-05-16](https://www.keypedia.com/records/483/qilu-synva-pharmaceutical-co-ltd/d5429ebd-a562-4752-85f4-d714c898528d) — source: FDA, date: May 16, 2025
- [FDA Inspection 1275186 - Qilu SYNVA Pharmaceutical Co. Ltd - 2025-05-16](https://www.keypedia.com/records/fda_inspections/qilu-synva-pharmaceutical-co-ltd/30ffc884-2b4e-4c89-a9dc-aed7726693e9) — source: FDA, date: May 16, 2025
- [FDA Inspection 1275186 - Qilu SYNVA Pharmaceutical Co. Ltd - 2025-05-16](https://www.keypedia.com/records/fda_inspections/qilu-synva-pharmaceutical-co-ltd/7398c1d2-13e4-4d0e-b30d-92df41dde77c) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 16, 2025
- [FDA Inspection 1115250 - Qilu SYNVA Pharmaceutical Co. Ltd - 2019-12-13](https://www.keypedia.com/records/fda_inspections/qilu-synva-pharmaceutical-co-ltd/98f9dfc4-68b0-4ac7-b1d5-463d73859013) — classification: No Action Indicated (NAI), source: FDA, date: December 13, 2019
- [FDA Inspection 1098879 - Qilu SYNVA Pharmaceutical Co. Ltd - 2019-07-26](https://www.keypedia.com/records/fda_inspections/qilu-synva-pharmaceutical-co-ltd/a2d93be4-63c0-40b0-a088-b95799038fdb) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 26, 2019
- [FDA Inspection 980987 - Qilu SYNVA Pharmaceutical Co. Ltd - 2016-06-17](https://www.keypedia.com/records/fda_inspections/qilu-synva-pharmaceutical-co-ltd/a52407b2-ed98-4b6b-b089-41bafd040439) — classification: No Action Indicated (NAI), source: FDA, date: June 17, 2016

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