FDA Inspection
Lighthouse For The BlindLighthouse For The Blind – FDA Inspection, Jun 30, 2014
Record Details
This FDA Inspection record concerns Lighthouse For The Blind, with an inspection on June 30, 2014, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Lighthouse For The Blind
- Inspection Date
- June 30, 2014
- Product Type
- Devices
View Company Profile
ID · ce05cda0-8e61-4ede-999b-cc2c3b61bca5
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 884504
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
7- 21 CFR 211.166(b)Adequate number of batches on stability
- 21 CFR 211.94(a)Reactive/Additive/Absorptive Containers/Closures
- 21 CFR 211.137(a)Expiration date lacking
- 21 CFR 211.25(a)GMP Training Frequency
- 21 CFR 211.25(b)Supervisor Training/Education/Experience
- 21 CFR 211.113(a)Procedures for non-sterile drug products
- 21 CFR 820.50Purchasing controls, Lack of or inadequate procedures
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Lighthouse For The Blind
7| Date | Classification | Office | Project area |
|---|---|---|---|
| May 7, 2025 | Not classified | Kansas City District Office | |
| July 14, 2022 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| June 13, 2018 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| April 17, 2018 | Not classified | Kansas City District Office | |
| April 8, 2015 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Lighthouse For The Blind
- FDA Inspection 1271438 - 2025-05-07
- FDA Inspection 1177559 - 2022-07-14
- FDA Inspection 1059389 - 2018-06-13
- FDA Inspection 1049210 - 2018-04-17
- FDA Inspection 922428 - 2015-04-08
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