Central Admixture Pharmacy Services, Inc.
Letter data
- Company
- Central Admixture Pharmacy Services, Inc.
- Recipient
- Thomas J. Wilverding | President | Central Admixture Pharmacy Services, Inc. | 6580 Snowdrift Road | Suite 100 | Allentown | , | PA | 18106-9331 | United States
- Issue date
- 2020-06-17
- Posted date
- Not available
- FDA office
- Division of Pharmaceutical Quality Operations I
- Subject
- Not available
- Product
- Drugs
- CMS ID
- 498479
- Reference number
- Not available
- FEI
- Not available
- Inspection dates
- 2018-07-30 to 2018-08-22
Normalized citations
21 CFR: 21-CFR-20.64(d)(3)21-CFR-PART-20
21 U.S.C.: None found
Related FDA links
No related FDA letter link is present in the source index.
Full source text
CLOSEOUT LETTER
Central Admixture Pharmacy Services, Inc.
MARCS-CMS 498479 —
June 17, 2020
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Delivery Method:
Certified Email
Product:
Drugs
Recipient:
Recipient Name
Thomas J. Wilverding
Recipient Title
President
Central Admixture Pharmacy Services, Inc.
6580 Snowdrift Road
Suite 100
Allentown
,
PA
18106-9331
United States
Issuing Office:
Division of Pharmaceutical Quality Operations I
United States
(973) 331-4900
Dear Mr. Wilverding:
We are enclosing a copy of the Establishment Inspection Report (EIR) for the inspection conducted at your facility, Central Admixture Pharmacy Services, Inc., located at 6580 Snowdrift Road, Suite 100, Allentown, PA 18106-9331, from July 30, 2018, to August 22, 2018, by the U.S. Food and Drug Administration (FDA). We are also releasing a copy of the Establishment Inspection Report (EIR)s for the inspections conducted August 29, 2016, to September 19, 2016, February 3, 2015 to February 11, 2015, and June 4, 2014, to June 11, 2014.
When the Agency concludes that an inspection is “closed” under 21 C.F.R. 20.64(d)(3), it will release a copy of the EIR to the inspected establishment.
The Agency continually works to make its regulatory process and activities more transparent for regulated industry. Releasing this EIR to you is part of this effort. The copy being provided to you comprises the narrative portion of the report; it may reflect redactions made by the Agency in accordance with the Freedom of Information Act (FOIA) and 21 C.F.R. Part 20. This, however, does not preclude you from requesting and possibly obtaining any additional information under FOIA.
If there is any question about the released information, please contact Yvette Johnson, Compliance Officer at
Yvette.Johnson@fda.hhs.gov
.
Sincerely,
/S/
Stephanie Durso, Compliance Branch Director
Office of Pharmacy Quality Operations, Division I
Content current as of:
06/23/2020
Regulated Product(s)
Drugs