# Shandong New Time Pharmaceutical Co. Ltd., Linyi, China – FDA Inspections

Source: https://www.keypedia.com/companies/shandong-new-time-pharmaceutical-co-ltd/470fe860-121a-4594-b9a5-e6bf05ce1926

> Inspection records and compliance data for Shandong New Time Pharmaceutical Co. Ltd. in Linyi. 4 FDA inspections on record, 1 Form 483, last inspected July 09, 2024.

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## Details

- Name: Shandong New Time Pharmaceutical Co. Ltd.
- FEI Number: 3006704412
- Business Operations: API MANUFACTURE, API/FDF ANALYTICAL TESTING, FDF MANUFACTURE, PACK
- Address Line 1: No. 1 North Outer Ring Road, Feixian
- City: Linyi
- Country Name: China
- Address: No. 1 North Outer Ring Road, Feixian, Linyi, China
- Country: China

## Related Documents

- [483 - Shandong New Time Pharmaceutical Co. Ltd. - 2024-07-09](https://www.keypedia.com/records/483/shandong-new-time-pharmaceutical-co-ltd/1ae1162b-59b7-4515-a05a-46d385e9b89f) — source: FDA, date: July 9, 2024
- FDA Inspection 1244268 - Shandong New Time Pharmaceutical Co. Ltd. - 2024-07-09 — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 9, 2024
- [483 - Shandong New Time Pharmaceutical Co. Ltd. - 2024-07-01](https://www.keypedia.com/records/483/shandong-new-time-pharmaceutical-co-ltd/74710a97-7da7-4a05-9544-dfcc9791cb9e) — source: FDA, date: July 1, 2024
- [FDA Inspection 1054213 - Shandong New Time Pharmaceutical Co. Ltd. - 2018-05-11](https://www.keypedia.com/records/fda_inspections/shandong-new-time-pharmaceutical-co-ltd/52a2304e-d72c-4c91-9a20-7a87b78b52fc) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 11, 2018
- FDA Inspection 967561 - Shandong New Time Pharmaceutical Co. Ltd. - 2016-03-25 — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 25, 2016
- [FDA Inspection 854834 - Shandong New Time Pharmaceutical Co. Ltd. - 2013-08-23](https://www.keypedia.com/records/fda_inspections/shandong-new-time-pharmaceutical-co-ltd/74a7d8b7-8974-4a13-9725-72ecbb3bd48f) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 23, 2013

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