# Repro Lab, Inc. - Inspection Records

Source: https://www.keypedia.com/companies/repro-lab-inc/8960714b-ecb8-4b1d-80ad-c0ad8cb96afe

> Inspection records and compliance data for Repro Lab, Inc. in New York, New York. Access full analysis and detailed observations.

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## Details

- Name: Repro Lab, Inc.
- FEI Number: 3000974212
- City: New York
- State: New York
- Country Name: United States
- Address Line 1: 332 E 30th St
- Zip Code: 10016

## Related Documents

- [483 - Repro Lab, Inc. - 2024-11-19](https://www.keypedia.com/records/483/repro-lab-inc/b44f205b-cb35-4b0e-a1e0-6f2bf37d5dfd) — source: FDA, date: November 19, 2024
- [FDA Inspection 1255573 - Repro Lab, Inc. - 2024-11-19](https://www.keypedia.com/records/fda_inspections/repro-lab-inc/14a1802d-30a7-4b9c-9b55-a256b7aad146) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 19, 2024
- [FDA Inspection 1172852 - Repro Lab, Inc. - 2022-06-24](https://www.keypedia.com/records/fda_inspections/repro-lab-inc/bdb143f3-9df6-4923-94f3-627dd7ffa029) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 24, 2022
- [FDA Inspection 1172852 - Repro Lab, Inc. - 2022-06-24](https://www.keypedia.com/records/fda_inspections/repro-lab-inc/bc873ebd-3e7d-400b-abba-444ca375fcdf) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 24, 2022
- [FDA Inspection 1172852 - Repro Lab, Inc. - 2022-06-24](https://www.keypedia.com/records/fda_inspections/repro-lab-inc/6b33767d-4ba0-4815-8440-662d34ff8260) — classification: No Action Indicated (NAI), source: FDA, date: June 24, 2022
- [483 - Repro Lab, Inc. - 2020-10-16](https://www.keypedia.com/records/483/repro-lab-inc/6b339c28-e6fe-47f9-be9d-ad6e831479a1) — source: FDA, date: October 16, 2020
- [FDA Inspection 1131538 - Repro Lab, Inc. - 2020-10-16](https://www.keypedia.com/records/fda_inspections/repro-lab-inc/99645c7a-4ce0-4bac-b0d6-3f8d6fcb046b) — classification: No Action Indicated (NAI), source: FDA, date: October 16, 2020
- [FDA Inspection 1131538 - Repro Lab, Inc. - 2020-10-16](https://www.keypedia.com/records/fda_inspections/repro-lab-inc/de28dd86-0fd5-49a5-ad6c-ff39caef65d4) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 16, 2020
- [FDA Inspection 1131538 - Repro Lab, Inc. - 2020-10-16](https://www.keypedia.com/records/fda_inspections/repro-lab-inc/cb1bc917-cc35-45f6-81a5-ae6097976713) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 16, 2020
- [FDA Inspection 1045046 - Repro Lab, Inc. - 2018-03-19](https://www.keypedia.com/records/fda_inspections/repro-lab-inc/e84b0b3b-f6c1-44a9-9b55-1b795fdd531d) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 19, 2018
- [FDA Inspection 1045046 - Repro Lab, Inc. - 2018-03-19](https://www.keypedia.com/records/fda_inspections/repro-lab-inc/019cbf60-bd6c-4161-948e-893b92572e74) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 19, 2018
- [FDA Inspection 961911 - Repro Lab, Inc. - 2016-03-08](https://www.keypedia.com/records/fda_inspections/repro-lab-inc/40330317-aa57-45bd-b4d0-311c314ed545) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 8, 2016

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