# FDA Inspection 1030256 - Gensynth Laboratories Private Limited - September 21, 2017

Source: https://www.keypedia.com/records/fda_inspections/gensynth-laboratories-private-limited/b4490c07-dccc-49a7-95c6-e35d8da98aa5
Source feed: FDA_Inspections

> FDA Inspection 1030256 for Gensynth Laboratories Private Limited on September 21, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1030256
- Company Name: Gensynth Laboratories Private Limited
- Inspection Date: 2017-09-21
- Classification: No Action Indicated (NAI)
- Project Area: Drug Quality Assurance
- Product Type: Drugs
- Office Name: Center for Drug Evaluation and Research

Company: https://www.keypedia.com/companies/gensynth-laboratories-private-limited/92f9eb19-bf70-439f-8d0b-8f7d622861db

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