# FDA Inspection 1080590 - Shandong Lukang Shelile Pharmaceutical Co., Ltd. - December 14, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/shandong-lukang-shelile-pharmaceutical-co-ltd/aa648476-7708-4b35-aad6-55cb6980417e
Source feed: FDA_Inspections

> FDA Inspection 1080590 for Shandong Lukang Shelile Pharmaceutical Co., Ltd. on December 14, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1080590
- Company Name: Shandong Lukang Shelile Pharmaceutical Co., Ltd.
- Inspection Date: 2018-12-14
- Classification: No Action Indicated (NAI)
- Project Area: Drug Quality Assurance
- Product Type: Drugs
- Office Name: Center for Drug Evaluation and Research

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Company: https://www.globalkeysolutions.net/companies/shandong-lukang-shelile-pharmaceutical-co-ltd/951ce05d-eb54-4085-9e1c-8fe979d9f0bb

Office: https://www.globalkeysolutions.net/offices/center-for-drug-evaluation-and-research/cd980d74-1cbf-4226-ba9a-9045324c236c