# FDA Inspection 1044270 - Post Surgical Manufacturing - March 06, 2018

Source: https://www.keypedia.com/records/fda_inspections/post-surgical-manufacturing/9672b49b-c35f-4cfe-9aab-ad8a5f8d98eb
Source feed: FDA_Inspections

> FDA Inspection 1044270 for Post Surgical Manufacturing on March 06, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1044270
- Company Name: Post Surgical Manufacturing
- Inspection Date: 2018-03-06
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1173309 - 2022-06-24](https://www.keypedia.com/records/fda_inspections/post-surgical-manufacturing/a4ab1adf-b456-4182-8b8f-a3b4606df7c9)
- [FDA Inspection 1173309 - 2022-06-24](https://www.keypedia.com/records/fda_inspections/post-surgical-manufacturing/605e7545-03bc-4f7e-8ea3-19da97ca5c67)

Company: https://www.keypedia.com/companies/post-surgical-manufacturing/3c9784ce-73f6-4f0e-bbba-54c3329b542d

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7
