# FDA Inspection 1020620 - Lydia Lane - July 25, 2017

Source: https://www.keypedia.com/records/fda_inspections/lydia-lane/2d0bae55-93c2-4ef9-bdba-f06728e1aad6
Source feed: FDA_Inspections

> FDA Inspection 1020620 for Lydia Lane on July 25, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1020620
- Company Name: Lydia Lane
- Inspection Date: 2017-07-25
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Bioresearch Monitoring
- Product Type: Drugs
- Office Name: Center for Drug Evaluation and Research

Company: https://www.keypedia.com/companies/lydia-lane/b378646a-e9a2-4c13-a72b-dfa5698c3bd6

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