Company
United StatesLitex Manufacturing, Inc, Glendale, CA – FDA Inspections
Inspection records and compliance data for Litex Manufacturing, Inc in Glendale, California. 3 FDA inspections on record, last inspected April 11, 2024.
Company Profile
This profile covers Litex Manufacturing, Inc based in Glendale, California, United States.
FDA Inspection History
- FDA inspections
- 3
- OAI
- 0
- VAI
- 0
- NAI
- 2
- Unclassified
- 1
- Form 483s
- 0
- Warning letters
- 0
First inspected August 13, 2018. Last inspected April 11, 2024.
FDA inspections (3)
| Date | Result | FDA center(s) | Insp. # |
|---|---|---|---|
| April 11, 2024 | Not classified | Medical Devices & Rad Health | 1238473 |
| August 5, 2021 | NAI | Medical Devices & Rad Health · Postmarket Assurance: Devices | 1148524 |
| August 13, 2018 | NAI | Medical Devices & Rad Health · Compliance: Devices | 1064722 |
FDA documents
No Form 483s, Warning Letters or EIRs on record.
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Company Information
Name
Litex Manufacturing, Inc
FEI Number
3010676465
Address
820 Thompson Ave Ste 9, Glendale, California 91201, United States
Country
United States
ID: 6e7e4274-e9c4-49f9-a01a-c9e9e8a2fc98