# CorneaGen - Boston - Inspection Records

Source: https://www.keypedia.com/companies/corneagen-boston/78964c02-d403-4377-8609-2434e1adaef8

> Inspection records and compliance data for CorneaGen - Boston in Waltham, Massachusetts. Access full analysis and detailed observations.

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## Details

- Name: CorneaGen - Boston
- FEI Number: 1000513310
- City: Waltham
- State: Massachusetts
- Country Name: United States
- Address Line 1: 300 Bear Hill Rd Fl 2
- Zip Code: 02451

## Related Documents

- [483 - CorneaGen - Boston - 2024-12-20](https://www.keypedia.com/records/483/corneagen-boston/8df31cfa-8379-47c9-8841-a09d6d074a37) — source: FDA, date: December 20, 2024
- [FDA Inspection 1257221 - CorneaGen - Boston - 2024-12-20](https://www.keypedia.com/records/fda_inspections/corneagen-boston/43ca6f6d-9fc0-4574-8a2c-ae5be00b98c8) — source: FDA, date: December 20, 2024
- [483 - CorneaGen - Boston - 2023-06-09](https://www.keypedia.com/records/483/corneagen-boston/83adf46e-9bd2-45b5-bdec-816b54f14c32) — source: FDA, date: June 9, 2023
- [FDA Inspection 1207719 - CorneaGen - Boston - 2023-06-09](https://www.keypedia.com/records/fda_inspections/corneagen-boston/1eb901f6-19b0-405f-8bab-144f6e931eea) — source: FDA, date: June 9, 2023
- [FDA Inspection 1121216 - CorneaGen - Boston - 2020-03-05](https://www.keypedia.com/records/fda_inspections/corneagen-boston/7a831ad9-4224-4fc8-8e7e-d1a6abb53f03) — classification: No Action Indicated (NAI), source: FDA, date: March 5, 2020
- [FDA Inspection 1121216 - CorneaGen - Boston - 2020-03-05](https://www.keypedia.com/records/fda_inspections/corneagen-boston/5eec9d36-3c8d-44a5-aa7e-c1847cb300ff) — classification: No Action Indicated (NAI), source: FDA, date: March 5, 2020
- [FDA Inspection 1121216 - CorneaGen - Boston - 2020-03-05](https://www.keypedia.com/records/fda_inspections/corneagen-boston/f1850371-f861-48c2-b3ae-2c4022fa55f5) — classification: No Action Indicated (NAI), source: FDA, date: March 5, 2020
- [FDA Inspection 1068364 - CorneaGen - Boston - 2018-09-12](https://www.keypedia.com/records/fda_inspections/corneagen-boston/172a0e4b-9bf1-44dc-833e-a9c9f79b973c) — classification: No Action Indicated (NAI), source: FDA, date: September 12, 2018
- [FDA Inspection 941531 - CorneaGen - Boston - 2015-08-20](https://www.keypedia.com/records/fda_inspections/corneagen-boston/426b84fd-7341-4f22-9b96-ca08363fba0c) — classification: No Action Indicated (NAI), source: FDA, date: August 20, 2015
- [FDA Inspection 824487 - CorneaGen - Boston - 2013-03-28](https://www.keypedia.com/records/fda_inspections/corneagen-boston/25aa4223-7973-4e2e-b56f-2b10ebc7d2d0) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 28, 2013
- [FDA Inspection 651853 - CorneaGen - Boston - 2010-03-12](https://www.keypedia.com/records/fda_inspections/corneagen-boston/f45df8ed-a789-45a8-9ad0-35bea33abb58) — classification: No Action Indicated (NAI), source: FDA, date: March 12, 2010

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- [Investigator](https://www.keypedia.com/people/anthony-n-onianwa/910dd164-8542-4259-b11f-ea3a3f6d7baa)
